Tuesday, February 25, 2014

$PLPL - Plandaí Biotechnology, Inc. Due diligence

PLPL - Plandaí Biotechnology, Inc.



PLPL Company Description
Plandaí Biotechnology, Inc. (OTCQB: PLPL): Plandaí Biotechnology, Inc. and its subsidiaries develop highly bioavailable, phytonutrient rich extracts, which are being utilized to deliver a new family of drugs to safely and affordably treat a multitude of diseases and conditions.

Plandaí Biotechnology controls every aspect of the process, from growing the raw materials on its farms in South Africa, to producing the patented pending Phytofare™ extracts in-house allowing the Company to guarantee the continuity of supply as well as quality control throughout Targeted industries for the Company's products include food and beverage, cosmeceutical, wellness, nutraceutical, anti-aging, and pharmaceutical. For more information, please visit http://www.plandaibiotech.com


PLPL Products and Benefits
Phytofare™



"BIOAVAILABILITY" can be defined as a measurement of the amount of compound absorbed into the bloodstream.

In the market today, green tea high purity EGCG extracts, with an average selling price of $500/kg, have poor bioavailability of between 1-10%. Plandaí proprietary plant extracts has shown, in published studies, to have increased bioavailability. We believe through our studies that this is between 60-80%, far exceeding anything currently available today.

Our extracts include but are not limited to, gallate catechins from green tea, (catechin gallate (CG),epigallocatechin gallate (EGCG), gallocatechin gallate (GCG), and epicatechin gallate (ECG); carotenoids (lycopene)from tomatoes, as well as citrus bioflavonoids and limonoids. Furthermore, Plandaí's gallate catechin extract will be the active ingredient in formulated products supporting weight loss, antiaging, the lowering of blood cholesterol, the regulation of high blood pressure and controlling diabetes 1 and 2.

This means, that Plandaí's extracts deliver a more meaningful and beneficial dose at highly competitive prices to the consumer, in wellness terms

The Northern American and European natural extracts market are emerging and in a state of intense competition. The shift towards natural ingredients is driving the expansion of the natural extracts market. Among the flurry of ingredients competing in the natural extracts market, green tea extracts is a pioneer and one of the most prominent success stories. (Frost & Sullivan Research, 2011)



Current Projects
Senteeko Estate

Plandaí Biotechnology, Inc., through its wholly owned subsidiaries, farms over 7500 acres of luscious land in the Mpumalanga province of South Africa.

It farms a whole fruit basket of produce which it uses in its creation of highly bioavailable extracts, ranging from citrus to avocado pears to most notably over 2000 acres of tea.
The tea plant, Camellia Sinensis, is an evergreen shrub or tree and can grow to heights of 30ft though for cultivation is pruned to heights of 2-5ft.

Farming in South Africa is like no other country in the world and because of this we needed to make sure that we stacked the deck in our favour and employed only the best as ever y step of the product creation pathway is critical. With that in mind, our farming team has over 100 years of experience in managing farms in Southern Africa.






Green Tea Project
Green tea is one of the most widely consumed beverages in the world, second only to water, and its medicinal properties have been widely explored.

The tea plant, Camellia Sinensis, is a member if the Theaceae family and black, oolong and green tea are produced from its leaves.

It's an evergreen shrub or tree and can grow to heights of 30ft though for cultivation is pruned to heights of 2-5ft.

Gallate Catechin Extract Project
Polyphenols found in tea are more commonly known as flavanols or catechins and comprise 30-40% of the extractable solids of dried green tea leaves. There are 8 catechins in green tea and of those 8 the gallate catechins are;
Catechin gallate (CG)
Epicatechin-3-gallate (ECG)
Epigallocatechin (EGC)
Epigallocatechin-3-gallate (EGCG)

A number of the catechin polyphenols that are abundant in tea are reputed to have pharmacologically active properties. Within the plant, catechins are purported to be involved in the defence against pathogens, including insects, bacteria, fungi and viruses. Protection against bacterial and viral infection has also been observed against human pathogens as well as a plethora of other heath parameters. Clinical immunology 2010; 137,347-356

Unlike most green tea extracts on the market which focus on selling EGCG, which is the dominant gallate catechin, Plandaí Biotechnology extract, Phytofare™-Gallate Catechin extract (GCE), utilizes all four gallate catechins so as to benefit from their synergistic qualities as when a single phytochemical is isolated as an ingredient for a nutraceutical or pharmaceutical related product the synergistic activities created by the presence of the whole phytochemical is lost and therefore bioavailability or absorption is reduced.
By ingesting catechins individually, irrespective of the purity, van Amelsvoort et al. demonstrated that the galloyation of the catechins EGCG, ECG, CG and GCG, whilst having higher activities than those catechins without the galloyl moiety (EGC and CG) have reduced their absorption and are the least absorbed.

http://www.plandaibiotech.com/images/senteeko-2013-tea3.jpg



Research and Development



Citrus
Citrus is recognized as one of the most healthful components of the human diet. Much of the contribution of citrus in human health and nutrition is attributed to secondary metabolites present in the fruit including antioxidants, (ascorbic acid, flavanones, simple phenolics, carotenoids), folate and pectin.
From 2006 through 2009 the company undertook extensive documented citrus fruit studies with Sunkist growers at the fruit juice processing facilities in Ontario and Tipton, California to recover pectin, bioflavonoids, limonoids and limonene. Scientific validation was undertaken by USDA and Chromadex Inc. These investigations included considerable research of Sunkist production of FDA pharmaceutical extracts during the 1950 -1960’s of citrus bioflavonoids, limonoids, pectin, limonene and vitamin C. Furthermore, 104 Sunkist clinical publications on citrus bioflavonoids delivered conclusive evidence of citrus bioflavonoid efficacy in blood, vascular and capillary studies.
Based on these findings, the company second phase project is to process lemon fruits during the period the tea business is dormant and to recover a number of specific botanical extracts as active ingredients for
THE TREATMENT OF INFLAMMATORY CONDITIONS WITH CITRUS BIOFLAVONOIDS
The corticosteroid blood level is enhanced
Treatment of rheumatic fever is improved by inclusion of citrus bioflavonoids in the therapeutic regimen.
The frequency and severity of rheumatic epistaxis (nose-bled) is diminished by citrus bioflavonoids
Maintenance of Capillary Integrity
Athletic Injuries and Citrus Bioflavonoid Therapy
The Common Cold
A total of eleven studies were reviewed on the use of citrus bioflavonoids (Hesperidin) and ascorbic acid in the treatment of upper respiratory infections. Clinical trials Saylor (1956) with ninety nine patients with allergic and vasomotor rhinitis, (which so closely resembles the common cold with it nasal symptoms) observed complete or partial relief from 69% using Hesperidin, Chalcone and Sodium in daily divided doses.
WL Macon. Journal of Industry, Medicine and Surgery November 1956. A total of one hundred and twenty one persons who met rigid qualifications as having a common cold were studied with sixty two receiving a combination of lemon-orange flavonate glycoside, and ascorbic acid; and the other fifty nine receiving aspirin, phenacetin and caffeine, a well known palliative for the cold.
A total of forty six patients (74.2%) reported on the second day of taking the medication that they achieved complete or substantial relief when taking the bioflavonoid combination. In comparison only 30% (50.9%) taking ACP’s, the best known palliative obtained similar relief.



Tomatoes
Farming and Recovery from tomatoes of Bioavailable Lycopene, phytoene and phytofluene extracts
Lycopene, phytoene and phytofluene are carotenoid pigments, found in tomatoes and other red fruits. They are natural fat-soluble pigments (red, in the case of lycopene) which are synthesized by some plants and micro-organisms but not by animals. They serve as an accessory light-gathering pigment and also aid in the protection of these organisms against the toxic effects of oxygen and light.
Lycopene, phytoene and phytofluene are the most common antioxidant carotenoids in the human body which are poorly absorbed by the human body. They are naturally present in human plasma and tissues in higher concentrations than the other carotenoids. Its levels are affected by several biological and lifestyle factors. Because of its lypophilic nature, its concentrates in low-density and very-low-density lipoprotein fractions of the serum and are also found to concentrate in the adrenal, liver, testes, and prostate. However, unlike other carotenoids, lycopene, phytoene and phytofluene levels in serum or tissues do not correlate well with overall intake of fruits and vegetables.
Cardiovascular diseases, along with cancer, are the main mortality causes in Europe and other developed countries. Strong correlative evidence suggests that lycopene may provide important protection against cardiovascular diseases and cancer. However the missing links in the chain are bioavailability, metabolism, and molecular mechanisms of biological activities that are still unknown. www.lycocard.com
In published studies conducted with tomato growers of California between 2006 -2009, and supported by scientific analysis and investigations by USDA, Chromadex Inc., Craft Laboratories and other specialized laboratories, Phytofare™ carotenoid extracts showed considerable evidence of increased accessibility of lycopene, phytoene and phytofluene to extraction procedures on tomato, while changing the stereoisomeric profile of the carotenoids to one that was highly bioavailable and therefore more beneficial to consumers.
Active ingredient for novel anti-malaria-drug
Most efforts to design vaccine interventions against malaria has been focused on the blood stage of the parasite, which is responsible for the symptoms of the disease; and it is only now that a number of successful studies with gallate catechins have provides a good scientific rationale to develop a preventive drug against the pre-erythrocyte stages of the malaria parasite.
It is in the specific target area that a bioavailable green tea gallate catechin extract has been identified as the potential active ingredient of inhibiting the hexose uptake processes in infected erythrocytes; which is the primary mechanism of their anti-malarial activity and may involve interaction with alternative higher affinity target/s. Gallate catechins are able to inhibit motility and cause cytotoxcity through the form of several hydrogen structures and ionic bonds with proteins and thereby modulating their 3D structure. It has been shown that gallate catechins bind to adhesion molecules on the parasite surface and this impairs gliding, leading to an inactivation of the surface proteins and rendering the parasites immotile.
In published in-vitro and animal model studies, gallate catechins have shown inhibiting qualities and anti-malaria properties.
Plasmodium sporozoites are the forms of the malaria parasite injected into the host during a blood meal of the mosquito; and they are then deposited within the skin, where they can move at a speed of around 1 µm/s. Some sporozoites can enter blood vessels and are transported to the liver, where they invade hepatocytes to differentiate into red blood cell invading merozoites.
Gallate catechins bind to the intercellular adhesion molecule 1 (ICAM 1) on the endothelium thus blocking the adhesion of Plasmodium infected erythrocytes.
Inhibits Plasmodium falciparum growth in vitro and potentiates the anti-malarial effects of artemisinin.
Mechanism of inhibition of an enoyl-acyl carrier protein reductase of Plasmodium falciparum, resulting in the inhibition of the fatty acid biosynthesis in the parasite.
Malaria Journal Slavic et al. Malaria Journal 2011, 10:165
In 2012, Plandai Biotechnology is scheduled to undertake in-vitro and animal studies to validate its extract, Phytofare™-GCE, as an active ingredient for novel anti-malaria drugs.



PLPL Key Company Management
Roger Duffield - President & CEO
Roger Duffield has a significant background in the development and management of start-ups, private and public companies, especially in the United States, Europe and South Africa. His previous contributions in the United States public sector include Klinair Technologies Inc. and Rhombic Inc. relating to energy and hydrocarbon technologies. Through his extensive involvement with research and development programs with a number of academic institutions, including Penn State, University of Southern California, University of Washington, and the University of Limerick, Ireland, he was awarded two honorary Russian doctorates in Natural Sciences from the University of Moscow and Novosibirsk. In 2001 the Foundation for International Services, California recognized a degree in BSc. Chemical Engineering.
In 2001 he co-founded Global Energy Solutions Corporation Limited, Dublin, Ireland, recently acquired by Plandaí Biotechnology, Inc., and in 2003, the USA-based Research Company, CRS Technologies Inc. Mr. Duffield now heads this group of companies specializing, through private and public investment in the farming and recovery of highly valuable botanical extracts with unique characteristics.

Callum Baylis-Duffield - Vice President
Mr. Callum Baylis-Duffield is a graduate in International Business with French (BA Hons) from the University of the West of England. From 2007-2010, he was employed by Johnson and Johnson UK as a marketing & sales manager of a proprietary surgical device. Since 2010 he has been exclusively employed by Global Energy Solutions as the Director of Marketing and Sales and for the past 18 months has been based in South Africa where he has been integral to bringing the proprietary extract to market.
Mr Baylis-Duffield has been involved with the research and development of the Plandaí’s proprietary emulsions since 2004 and has worked extensively with the USA scientific team.

PLPL Contact Info
Plandaí Biotechnology, Inc.
2226 Eastlake Avenue East
#156
Seattle, WA 98102
Australia

Website: http://www.plandaibiotech.com
Phone: 435-881-8734
Email: info@plandaibiotech.com

PLPL SEC Filings
http://www.otcmarkets.com/stock/PLPL/filings

PLPL Headlines
http://finance.yahoo.com/q/h?s=PLPL+Headlines

Investigate more about PLPL @ http://www.otcmarkets.com/stock/PLPL/quote for more due diligence.








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$LIVE - LiveDeal Inc. - Nasdaq Super Due Diligence


$LIVE - LiveDeal Inc.

 





Common stock trades on the NASDAQ Capital Market under the symbol "LIVE"

LIVE Company Description
About LiveDeal Inc.
LiveDeal Inc. provides marketing solutions that boost customer awareness and merchant visibility on the Internet. LiveDeal operates a deal engine, which is a service that connects merchants and consumers via an innovative platform that uses geo-location, enabling businesses to communicate real-time and instant offers to nearby consumers. In November 2012, LiveDeal commenced the sale of marketing tools that help local businesses manage their online presence under the Company's Velocity Local™ brand. LiveDeal continues to actively develop, revise, and evaluate these products and services and its marketing strategies and procedures. For more information, visit http://www.livedeal.com

$LIVE LiveDeal Video - Restaurant deals happening near you right now

http://www.youtube.com/watch?v=Hy7FPwfLSOA&feature=youtu.be&a


LiveDeal is the world's first deal engine—a real-time, online marketplace that connects you with local restaurants that are offering deals right now. Offers found on LiveDeal are all limited-time offers happening at that moment, or 'live'. Find exclusive deals and redeem them at your favorite local restaurant instantly. Take advantage of promotions and specials that are designed to entice you into local establishments. They help you save today and everyday.

LiveDeal (NASDAQ: LIVE) has been a publicly traded company since founded in 2003.

ARE YOU A RESTAURANT OWNER?
REACH MORE LOCAL CUSTOMERS WITH ON-DEMAND DISCOUNTS!


Avoid the Middleman
Promote your restaurant on LiveDeal and transact directly with your customer. Our users don't buy or pay for vouchers online, so we never hold funds on your behalf. Start realizing an immediate profit boost the moment customers start walking through your doors to redeem their deal.

Customize Your Local Offer
Run deals that are valid only at the locations you choose. Boost traffic at slower branches without overburdening other bustling locations. With superior geo-targeting capabilities, LiveDeal can publish discounts that are visible only to users within a certain radius of your live promotion.

Manage Your Traffic
LiveDeal puts you in control of the maximum number of users that can claim your voucher before a deal is sold out. Once all of your vouchers are claimed, your deal expires. You will never have to worry about your restaurant being understaffed or overcrowded again.

Just cap the voucher limit to 5, 10, or any quantity you can comfortably accommodate. When patrons experience VIP service, they're more likely to become repeat customers and spread glowing word-of-mouth recommendations.

Basic Advertising is Free?
Let your competitors pay to advertise. Quite possibly the best part of LiveDeal is the price for basic listings, or lack thereof. Publish real-time deals on LiveDeal and avoid revenue shares, sign-up fees, posting fees, and annual fees. Why not pass this savings on to LiveDeal local patrons by offering even more appealing bargains?
http://livedeal.com/pressroom/



LIVE Products and Services
What is livedeal.com?
livedeal.com is a unique, real-time "deal engine" connecting merchants with consumers. The Company believes that it has developed a first-of-its-kind web/mobile platform providing restaurants with full control and flexibility to instantly publish customized offers whenever they wish to attract customers. The website includes a number of user and restaurant-friendly features, including:
an intuitive interface enabling restaurants to create limited-time offers and publish them immediately, or on a preset schedule that is fully customizable;
state-of-the-art scheduling technology giving restaurants the freedom to choose the days, times and duration of the offers, enabling them to create offers that entice consumers to visit their establishment during their slower periods;
advanced publishing options allowing restaurants to manage traffic by limiting the number of available vouchers to consumers;
superior geo-location technology allowing multi-location restaurants to segment offers by location, attracting customers to slower locations while eliminating potential overcrowding at busier sites; and
a user-friendly mobile and desktop web interface allowing consumers to easily browse, download, and instantly redeem "live" offers found on livedeal.com based on their location.
Restaurants can sign up to use the LiveDeal platform at the Company's website http://www.livedeal.com

LIVE Key Company Management
LiveDeal CEO Jon Isaac
Mr. Jon Isaac has been the President at LiveDeal, Inc. since January 20, 2012 and served as its Chief Executive Officer. Mr. Isaac Founded The Isaac Organization. Mr. Isaac has successfully closed on several, multi-faceted real estate transactions, including those involving the U.S. federal government and other publicly traded companies. Mr. Isaac has funded and added value to numerous publicly-traded companies. Mr. Isaac has been a Director of LiveDeal, Inc. since December 12, 2011. He has Economics and Finance Degree from the University of Ottawa, Canada.
http://investing.businessweek.com/research/stocks/people/people.asp?ticker=LIVE

LIVE Interview script with Jon Isaac, CEO and President of LiveDeal
http://socialhospitality.com/2013/10/livedeal-real-time-online-marketplace/#sthash.MwOMsAkh.dpuf

LIVE Contact Info
LiveDeal Inc.
2490 East Sunset Road
Suite 100
Las Vegas, NV 89120

Phone: 702-939-0230

$LIVE LiveDeal Inc. on Twitter https://twitter.com/LiveDealInc

$LIVE LiveDeal Inc. on Facebook https://www.facebook.com/LiveDeal

LIVE SEC Filings
http://www.otcmarkets.com/stock/LIVE/filings

LIVE Headlines
http://finance.yahoo.com/q/h?s=LIVE+Headlines

Investigate more about LIVE @ http://www.otcmarkets.com/stock/LIVE/quote for more due diligence.

Nuvilex, Inc. (OTCQB: $NVLX ) due diligence, bio cancer research company

Nuvilex, Inc.



About Nuvilex, Inc. (OTCQB: NVLX): Nuvilex, Inc. is an international biotechnology firm focused on developing and preparing to commercialize treatments for cancer, diabetes and other diseases based on the live, therapeutically valuable, encapsulated cells platform. The Company is leveraging its cancer biology and clinical oncology research experience and expertise, particularly for use in oncology treatments, in addition to initiating oncology applications of medical marijuana. 

For more information visit: http://www.nuvilex.com



RESEARCH & DEVELOPMENT of NVLX

Subsidiary, Medical Marijuana Sciences, Inc., is dedicated to the development of cancer treatments based upon the well-known chemical constituents of marijuana. Nuvilex is exploring ways in which the Cell-in-a-Box(TM) technology may play a role in these efforts


NVLX LIVE-CELL ENCAPSULATION RESEARCH & DEVELOPMENT



The live-cell encapsulation technology employed by Nuvilex is a way to enclose living cells in protective “cocoons” about the size of the head of a pin - we do not encapsulate drugs, but living cells. Each capsule can enclose approximately 10,000 cells; this number can differ depending upon the size of the cells encapsulated. The cell encapsulation technology used by Nuvilex can be classified as a “platform” upon which treatments for different indications may be built.

Depending on the type of cells used, the encapsulated cells can be employed in developing treatments for serious, debilitating and even deadly diseases. Nuvilex’s primary interests in the use of the live-cell encapsulation technology are for the development of treatments for various cancers and for diabetes.

Our live-cell encapsulation differs from that done by others in that the capsules that enclose the cells are made primarily of cellulose whereas others use substances such as alginate (a seaweed derivative), agarose, or chitosan, to name three. Because of this, the capsules are very robust and can withstand various external forces and this allows them to be implanted using needles or catheters without damage. Also, because they are made principally of cellulose, the capsules are essentially bio-inert in humans, so they do not degrade even after being present in the body for over two years.

The capsules contain pores that allow essential nutrients to enter and waste products and beneficial substances produced by the encapsulated cells to leave. Therefore, the cells inside the capsules can live and function for long periods of time after implantation. However, the pores are not large enough to permit the cells to leave the capsules or large enough to allow any cells of the body’s immune system to enter the capsules and destroy the encapsulated cells.

Even after more than two years in the body, no immune or inflammatory response is caused by the capsules themselves or by the cells within the capsules. In addition, the presence of the capsules does not cause fibrous overgrowth from, or other damage to, tissues nearby or surrounding the capsules.

Cells encapsulated using our technology can be stored frozen at -80°C or lower for long periods of time and then successfully thawed for use; this also allows for shipment of encapsulated cells to distant locations. Large-scale manufacturing of encapsulated cells using our technology has already been carried out according to GMP (Good Manufacturing Practice) conditions – a necessity for ultimately attaining marketing approval from drug regulatory authorities such as the U.S. FDA and the EMEA in Europe.

Nuvilex has recently acquired worldwide exclusive rights to the live cell-encapsulation technology described above from SG Austria Pte. Ltd. for the development of treatments for any and all types of cancer. The rights to use the cancer drug-activating cells (22P1G cells) that will be part of Nuvilex’s treatment for advanced pancreatic cancer (see Pancreatic Cancer section of this website) were also acquired. The acquisition of rights to use this live-cell encapsulation technology for the development of treatments for insulin-dependent diabetes is being finalized.

NVLX PANCREATIC CANCER RESEARCH & DEVELOPMENT



According to the American cancer Society, in the US alone, approximately 45,000 new cases of pancreatic cancer are expected to be diagnosed this year and about 38,000 people are predicted to die from the disease; it is the leading cause of cancer deaths in the US and worldwide. Often pancreatic cancer is not diagnosed until it has reached an advanced stage. By this time, the cancer cannot be removed surgically, is often resistant to radiation therapy or chemotherapy, and has spread (metastasized) to other organs in the body. Because of this, the average survival of patients with advanced, inoperable pancreatic cancer is given in terms of weeks or months, not years.

To date, there has only been one anticancer drug approved (in 1997) for use by the US FDA as a single agent for the treatment of advanced pancreatic cancer, namely GEMZAR®, also known as gemcitabine. Since 2000, more than 30 pivotal (for drug marketing approval) late-phase clinical trials have been carried out in an attempt to improve upon the effectiveness of gemcitabine against advanced pancreatic cancer by adding other drugs to it. Only a very few of these trials have even been moderately successful.

One of the success stories was the combination of gemcitabine with TARCEVA® (erlotinib). In the Phase III pivotal trial of that combination, the one-year survival rate for the gemcitabine/TARCEVA® combination was 24% as compared to 17% for a gemcitabine/placebo combination. In 2005, the FDA approved the gemcitabine/TARCEVA® combination as first-line therapy for advanced, metastatic pancreatic cancer.

The results of the second successful Phase III trial of a gemcitabine-containing combination were reported in January 2013. Here, the combination of ABRAXANE® plus gemcitabine was compared to gemcitabine alone in patients with advanced pancreatic cancer. ABRAXANE® is a formulation of nanoparticle-albumin-bound paclitaxel (TAXOL®). In this trial, when compared to gemcitabine alone, the ABRAXANE®/gemcitabine combination improved both median survival and one-year survival rate by about 30% and 59%, respectively. On September 6 2013, the combination of ABRAXANE® plus gemcitabine was approved by the FDA as first-line treatment for advanced, metastatic pancreatic cancer and replaced the gemcitabine/TARCEVA® combination as the “gold standard” for the treatment of the disease

A four-drug combination known as FOLFIRINOX (5-fluorouracil, leucovorin [WELLCOVORIN®], ironotecan [CAMPTOSAR®], and oxaliplatin [ELOXATIN®] is also fairly widely used to treat advanced pancreatic cancer. But, as for gemcitabine itself, and the gemcitabine/TARCEVA® and ABRAXANE®/gemcitabine combinations, FOLFIRINOX use carries with it severe drug-related side effects.

Nuvilex’s pancreatic cancer treatment consists of the use of a proprietary cellulose-based live-cell encapsulation technology together with the long-known and widely used anticancer drug ifosfamide (IFEX®). Ifosfamide is a prodrug that must be activated to its cancer-killing form for it to be effective; this usually occurs in the liver. Ifosfamide is administered intravenously (systemically), and like all anticancer drugs given this way, can cause drug-related toxicities in organs of the body unrelated to the tumor itself. The 22P1G cells encapsulated are capable of converting ifosfamide into its cancer killing form. The cells contain high levels of activity of one of the components of the cytochrome P450 enzyme system known as CYP2B1. The cytochrome P450 enzyme system is found in the liver and is responsible for the metabolism of lipids, steroid hormones, drugs, and other toxic substances. In actual practice, the pancreatic cancer treatment consists of first implanting the capsules containing the ifosfamide-activating cells through the use of radiography and then giving ifosfamide by its usual route of administration.

In a Phase I/II open-label, prospective, single-arm clinical trial, the live-cell encapsulation/ifosfamide combination was used to treat patients with advanced, inoperable pancreatic cancer. Fifty-one patients were originally “screened” for the trial; of these, 17 were enrolled in the study. Other patients were excluded from enrollment for therapy because of previous chemotherapy, previous pancreatic surgery, poor overall health, unwillingness to participate, or death prior to the start of the trial. Of the 17 patients initially enrolled in the study, 14 were ultimately treated.

Each patient in the trial received a single implantation of approximately 300 capsules (each capsule contained approximately 10,000 ifosfamide-activating cells), except for one patient who received 250 capsules, in the blood supply to the pancreas near that organ and thus the tumor itself; this was followed by two courses of therapy with ifosfamide at one-third of the dose normally used. Capsules were implanted on day 0 of treatment. After monitoring the patients on day 1, ifosfamide administration at a dose of 1 g/m2 of body surface area occurred on day 2 as a one-hour intravenous administration for three consecutive days; this was accompanied by the administration of the uroprotectant MESNA (also known as UROMITEXAN® or MESNEX®), as is normally the case when ifosfamide is used (the dose-limiting toxicity with ifosfamide is known to be damage to the urinary tract). Administration of ifosfamide was repeated on days 25-27; except for two patients who only received the initial course of treatment with ifosfamide. In addition a “quality-of-life” questionnaire was used for all 14 patients to document the clinical benefit of the treatment.

NVLX Results obtained in the clinical trial were compared with historical data for gemcitabine and included:

-median survival time of 44 weeks (after diagnosis) with the cell encapsulation/ifosfamide treatment as compared to 28 weeks with gemcitabine;
-doubling of the one-year survival rate – 36% with our treatment vs. 18% with gemcitabine;
-tumor volume was reduced 25-50% in 4 of the 14 treated patients and remained stable in the remaining patients;
-no serious drug-related side effects with the encapsulated cell/ifosfamide treatment whereas serious and very serious side effects were reported with gemcitabine; the lack of serious side effects using our treatment is probably related to the use of “lower than normal” doses of ifosfamide;
-limited side effects and reduced cancer pain intensity led to a generally increased ‘quality of life” for the majority of patients.

In a “worst case” scenario, some clinical benefit was seen in 50% of patients and in a “best case” scenario, this number increased to 71%; none of the patients who experienced a clinical benefit required and increase in their pain medication. In addition, no deleterious effects were seen that could be attributed to the presence of the capsules or the encapsulated cells; this observation testifies to the ability of the capsules to protect the cells inside them from attack and rejection by the body’s immune system for significant periods of time.

Reports of the Phase I/II trial of the cellulose-based live-cell encapsulation/ifosfamide combination in patients with advanced, inoperable pancreatic cancer have been published in reputable, peer-reviewed, scientific journals. The journal citations for the published articles are:

1. Löhr M., Hoffmeyer A., Kröger J-C., Freund M., Hain J., Holle A., Karle P., Knöfel W.T., Liebe S., Müller P., Nizze H., Renner M., Saller R.M., Wagner T., Hauenstein K., Günzburg W.H., and Salmons B. Microencapsulated cell-mediated treatment of inoperable pancreatic carcinoma. THE LANCET, Vol. 357, p. 1591 (2001).

To view the above-cited trial report click here. http://www.thelancet.com/journals/lancet/article/PIIS0140-6736%2800%2904749-8/abstract. The website in this link requires that readers register before the article can be viewed – the process is simple and free.

2. Löhr M., Kröger J-C., Hoffmeyer A., Freund M., Hain J., Holle A., Knöfel W.T., Liebe S., Nizze H., Renner M., Saller R., Müller P., Wagner T., Hauenstein K., Salmons B., and Günzburg W.H. Safety, feasibility and clinical benefit of localized chemotherapy using microencapsulated cells for inoperable pancreatic cancer in a phase I/II trial. Cancer Therapy, Vol. 1, p. 121 (2003).

To view the above-cited trial report click here. http://www.cancer-therapy.org/CT/v1/A/13%20%20L%C3%B6hr%20et%20al,%20121-131%20cop.pdf

To summarize, local implantation of encapsulated cancer prodrug-activating cells near the tumor increases the locally available amount of the activated anticancer drug directly in the pancreatic tumor. This ensures high efficacy of the anticancer drug with lower doses of that drug and thus also reduces the unpleasant and often serious side effects of the chemotherapy.

On the basis of the above positive clinical trial results, Nuvilex is making preparations for conducting a late-phase, randomized, multi-site, multinational clinical trial in which our treatment will be compared “head-to-head” with gemcitabine in patients with advanced, inoperable pancreatic cancer. Initial activities underway include the “scaling-up” of the production of ifosfamide-activating cells to ensure that sufficient numbers will be available for encapsulation to complete the trial, and the establishment of a GMP-compliant facility in which to conduct the encapsulation of the cells, as well as having the requisite equipment manufactured with which to do so. In addition, Contract Research Organizations (CROs) are being evaluated to assist in all aspects of the clinical trial.

NVLX BREAST CANCER RESEARCH & DEVELOPMENT



For 2013, the American Cancer Society estimates that more than 230,000 cases of breast cancer will be diagnosed in the US alone and more than 40,000 individuals are predicted to die from this disease; about 99% of these are females. Worldwide, breast cancer is the fifth most common cause of cancer deaths, and is second only to lung cancer in overall prevalence; more than one million new cases are diagnosed each year. After skin cancer, breast cancer is the most common of all cancers among women both in the US and worldwide. The breast cancer market (in major markets) has been predicted to be almost $ 11 billion by 2018.

From 5-10% of all breast cancers have a hereditary link, with women who have a first-degree relative with breast cancer being most at risk for developing the disease. Between 20 and 25% of hereditary breast cancers and 5-10% of all breast cancers result from mutations of the breast cancer suppressor genes BRCA1 and/or BRCA2. A particularly well-known form of breast cancer, accounting for about 20-25% of non-hereditary forms of the disease, is one in which the HER2 (human epidermal growth factor) gene is overexpressed; it is known as HER2-positive, or HER2+, breast cancer. Normally, breast cells contain two copies of the HER2 gene, but in HER2+ breast cancer cells, many more copies of the gene are present; this results in a greatly increased amount of HER2 receptors on the outside of HER2+ breast cancer cells than is normally the case. This overexpression of HER2 receptors has been exploited in the development of two blockbuster monoclonal antibody drugs, HERCEPTIN® (trastuzumab) and PERJETA® (pertuzumab); these are used in various combinations against only HER2+ breast cancer..

According to the American Cancer Society, 10 different chemotherapeutic drug combinations have been widely used for years to treat various forms of breast cancer – particularly non-HER2+ breast cancer. Of these, three can be classified as two-drug combinations, six as three-drug combinations, and one is a four-drug combination. Nine of these 10 combination chemotherapies use the anticancer drug cyclophosphamide (CYTOXAN®) as one of the components of the combination.

Cyclophosphamide is a “sister” drug to ifosfamide, the anticancer agent used in the mid-phase clinical trials in patients with advanced, inoperable pancreatic cancer that employed the Company’s cell encapsulation-based treatment. Both drugs are classified as “prodrugs” and must be activated (converted to their cancer-killing form) for them to be effective; this usually takes place in the liver. The same enzyme system in the liver activates both cyclophosphamide and ifosfamide.

Given the effectiveness of Nuvilex’s pancreatic cancer treatment in which cells capable of activating ifosfamide were encapsulated in cellulose-based microcapsules. The same ifosfamide-activating enzyme as that found normally found in the liver was genetically increased in activity in the encapsulated cells. Because ifosfamide and cyclophosphamide are activated in the same way, the same type of encapsulated cells was used in a veterinary early/mid-phase clinical trial in which dogs with spontaneously-occurring mammary tumors were treated with either cyclophosphamide alone or with the combination of encapsulated cells plus cyclophosphamide.

Spontaneously-occurring mammary tumors in dogs represent a good animal model system for the testing of anticancer drugs designed to be used against breast cancer in humans. Cyclophosphamide was chosen for the study rather than ifosfamide because it is often used to treat mammary tumors in dogs and because it is a component of most combination chemotherapy regimens used against breast cancer in humans.

In the study itself, encapsulated cyclophosphamide-activating cells were implanted into the tumors and then cyclophosphamide was administered intravenously, at its usual dose, in four treatments 2,9,22, and 29 days later. As in the pancreatic cancer clinical trials in humans, the capsules and the cells within them were well tolerated – no “safety” issues were seen. Dogs that received the cell encapsulation/cyclophosphamide combination exhibited a greater degree of tumor shrinkage than dogs that received cyclophosphamide alone.

One dog had two spontaneously-occurring mammary tumors. In that animal, encapsulated cells were implanted in only one of the tumors. The tumor that did not receive the encapsulated cells, and thus was treated with cyclophosphamide alone, shrank in size by 14% as compared to the 70% shrinkage seen with the tumor that was treated with the combination of cell encapsulation plus cyclophosphamide.

The results of this study indicate that the combination of cellulose-based live-cell encapsulation and cyclophosphamide may prove to be of significant benefit for the treatment of breast cancer in humans, by optimizing the cancer-killing activity of cyclophosphamide, when that drug is used in various combination chemotherapy regimens for the disease.

NVLX DIABETES RESEARCH & DEVELOPMENT



The International Diabetes Federation estimates that more than 370 million people worldwide have diabetes and that about 190 million remain undiagnosed. Therefore, many millions of people are subject to the debilitating, and even deadly, complications of this disease; these include heart disease, vision loss, kidney disease, and nerve damage, particularly to the feet and legs, which may ultimately necessitate amputation. The worldwide market for diabetes treatments has been projected to reach $65 billion by 2020.

Diabetes is characterized by sustained high levels of sugar (glucose) in the blood. Glucose is a source of energy for all cells in the body. Normally, the levels of glucose are regulated by insulin produced by β-cells of the Islets of Langerhans (islet cells or islets)within the pancreas.

There are two “types” of diabetes:

Type 1 Diabetes - About 5-10% of diabetics have Type 1 disease,formerly called juvenile onset diabetes because it mainly occurs in those 20 of age or younger. Here, the pancreas, having been damaged by autoantibodies, is incapable of producing insulin. As a consequence, these individuals require insulin daily given either by injection or by an insulin “pump.”

Type 2 Diabetes - The majority of diabetics have Type 2 diabetes, also known as adult onset diabetes because it is not usually diagnosed until individuals are 35 years of age or older. In Type 2 diabetes, either the pancreas produces too little insulin or the insulin produced cannot be used efficiently by the body - a phenomenon known as “insulin resistance.” Insulin resistance develops because of many factors, including genetics, obesity, increasing age, and the presence of high blood sugar for a long time. Type 2 diabetes, at least in its early stages, can be “treated” by such things as increased exercise, weight loss, and by anti-diabetic drugs, but over time, many of these individuals may also require insulin administration either with or without anti-diabetic medications.

One way to reduce diabetics’ dependence on insulin administration is through the use of pancreatic islet cell transplantation. In a ground-breaking study known as the “Edmonton Protocol,” islet cells from human cadavers were transplanted into insulin-dependent diabetics. However, cadaveric islet cell transplantations are problematic because (a) the supply of islet cells is limited and (b) potent and expensive immunosuppressive drugs must be administered for the remainder of diabetic patients’ lives or for as long as islet cell transplantations are used.

In an effort to avoid the use of islet cells from human cadavers, islet cells from pigs have been employed instead. This approach, known as xenotransplantation, has been used with alginate-encapsulated pig islets and has shown some success. However, the integrity of capsules composed of alginate have been shown to degrade with time; this allows for immune system attack on the transplanted pig islets and necessitates additional transplantations. Furthermore, drug regulatory authorities have been resistant to such interspecies transplantations of tissues in the past. Finally, the use of pig islets requires that a population of “germ-free” pigs be maintained – an expensive and problematic situation.

In a “proof-of-principle” study, cellulose-based capsules (produced in the same way as the capsules used in the pancreatic cancer clinical trials) containing live pancreatic islet cells from pigs were implanted into diabetic rats. Within a very short time, the blood glucose levels of the rats became normalized and remained that way for the 6-month duration of the study. Because of the robustness and longevity (over two years in humans in the pancreatic cancer trials done to date) of the cellulose-based capsules, no immunosuppressive drugs were necessary. Finally, when the capsules were removed from the rats at the end of the study, the cells that had been encapsulated were found to be fully viable and capable of responding to changes in glucose levels in their surroundings. This study illustrates the true platform nature of the cellulose-based live-cell encapsulation technology in developing a type of artificial pancreas.

Because of the positive results from the above proof-of-principle study, the Company plans additional expanded animal studies (longer duration, more animals) in which insulin-producing cells are encapsulated in its cellulose-based capsules. If the results from the proof-of-principle study are confirmed, this would ultimately lead to human clinical trials in diabetic individuals.

NVLX Management


Kenneth L. Waggoner, Chief Executive Officer and President:
Kenneth L. Waggoner has almost four decades of experience in management, business, operations and law. Mr. Waggoner started his career as an attorney in private practice. Notably he was a senior partner with Brobeck, Phleger and Harrison, named one of the top two law firms worldwide that provide services to biotechnology clients including Chiron, Amgen, Biogen Idec, Sangamo, Ligand, DepoTech and many others. He was the Managing Partner of Brobeck’s Los Angeles office. Mr. Waggoner was also a member of the Executive Committee for almost ten years and on the Policy Committee for numerous years managing Brobeck’s worldwide operations with annual revenues in excess of $750,000,000. While at Brobeck, Mr. Waggoner was the Co-Chairman of Brobeck’s world-wide Environmental Law Group.

Further highlights of Mr. Waggoner’s career include leadership and legal positions with several start-up companies during the last several years as well as working with Fortune 500 companies most of his professional career. During his tenure with Chevron, Mr. Waggoner served as the Vice President and General Counsel of its Global Downstream operations where he was responsible for the overall management of legal services to the North American, Latin American, Europe and Asian Products Companies. At Chevron he led a successful restructuring of the company’s international Legal Department following Chevron’s acquisition of Texaco.

Mr. Waggoner received his Juris Doctorate. with honors in 1973 from Loyola University School of Law in Los Angeles.
Dr. Robert F. Ryan, Chief Scientific Officer:

Dr. Robert F. Ryan was named Chief Scientific Officer. Dr. Ryan has broad scientific experience in biochemistry, cell and molecular biology, human genetics, novel therapies, and basic and clinical cancer research, having received his Masters in Biochemistry, Cell and Molecular Biology at The Medical College of Georgia, studying sickle cell anemia. He received his Ph.D. in Molecular Genetics at Thomas Jefferson University characterizing DNA and RNA binding properties of zinc finger proteins. Through his extensive training, his experiences extend across the fields of aging, hemoglobinopathies, gene expression, human diseases, DNA, RNA, proteins and their interactions, stem cell research and applications, oncology, clinical protocols and therapies.

Professionally, Dr. Ryan has become a pioneer in the field of emerging biotechnology, specializing in assisting small companies with insight and bringing products to market through the rigorous FDA approval process. Since 2002, Dr. Ryan served as the Chief Executive Officer of RFR Consulting where he focused on helping businesses in the biotech industry through providing information, grant writing, business management, scientific guidance, FDA regulatory advice, advising investors, and investment acquisition opportunities. With 25 years experience including excellent training at the Wistar Institute, NIH, and NCI, he has participated in basic and clinical investigations and has published and edited research articles in several peer-reviewed journals.

http://www.nuvilex.com/management

SHARE HOLDER info: http://www.nuvilex.com/shareholder-info

NVLX International Corporate Headquarters
Nuvilex, Inc.
Meadows Corporate Park I
12510 Prosperity Blvd., Suite #310
Silver Spring, MD 20904
Phone: (877) 598-7616
Fax: (917) 595-2850
email: info@nuvilex.com

NVLX Headline Press Releases
http://finance.yahoo.com/q/h?s=NVLX+Headlines

BFLX SEC Filings
http://www.otcmarkets.com/stock/NVLX/filings

Investigate more about NVLX @ http://www.otcmarkets.com/stock/NVLX/quote for more due diligence.






$SUBB - Suburban Minerals Corp. Mega Due diligence Updated 2.24.14

SUBB - Suburban Minerals Corp



SUBB Company Description
Suburban Minerals Corp is a publicly traded company seeking to acquire and operate producing mines in challenging world economies, to provide the highest return on investments and create long term sustainable value to its shareholders.

Suburban Minerals Corp. trades on the OTCPink under the Ticker Symbol: SUBB and is headquartered in Henderson, Nevada.

SUBB Products and Services
SUBB Signs Acquisition to acquire rights to a Diamond Concession in the Republic of Central Africa
HENDERSON, NV--(Marketwired - Jan 30, 2014) - Suburban Minerals Corp. (OTC Pink: SUBB) announced today the signing of the acquisition agreement to acquire the exploration, production and commercialization rights to a Diamond Concession in the Republic of Central Africa.

According to the agreement, the company will acquire the Diamond Concession Rights located in the Republic of Central Africa for a total of 300 million restricted common shares of Suburban Minerals at a price of $0.20 and 10 million convertible preferred shares at a price of $10.00, establishing the acquisition price at $160 million USD. Each Preferred share is convertible into 50 common shares of the company upon Suburban Minerals receiving financing in the amount of $300 million USD from the Intergovernmental Organization.

In addition to the issuance of common and preferred shares, Suburban Minerals will pay a royalty of 2.5% of gross profits to the Intergovernmental Organization and 10% of the operational budget up to a maximum payment of $500,000 yearly.

The company expects to complete due diligence, satisfy all regulatory requirements and close the acquisition on or before February 28, 2014.

"This is another significant milestone for our company, our shareholders and stakeholders," said Tim Sperling, President & CEO of Suburban Minerals Corp. "This acquisition is the stepping stone for the creation of sustainable value."
http://finance.yahoo.com/news/suburban-minerals-signs-diamond-concession-120000829.html?soc_src=mediacontentstory

Diamond Information
Diamonds possess a value, both visually and economically that has endured with the passing of time. The first diamonds discovered were found in a riverbed in India around 800 BC as a result of a volcanic source that has never been found. Royalty were recorded wearing diamonds as early as 1300 AD. The first engagement ring is said to be have been given by Archduke Maximilian of Austria to Mary of Burgundy in 1477 starting the tradition of diamond engagement rings.

In 1867, a 21 carat stone discovered on the banks of the Orange River, South Africa, started a great diamond rush. Between 1870 and 1891, no less than six kimberlite pipes were discovered in Kimberley.

Natural diamonds are formed at certain conditions of high-pressure and high temperature that only exist at depths of 140 to 190 kilometers (90 to 120 miles) in certain parts of the Earth’s mantle. The correct combination of temperature and pressure required to form diamonds is only found in the thick, ancient, and stable parts of continental plates called cratons. Diamonds formed at depth are brought close to the surface through deep volcanic eruptions, forming igneous rocks known as kimberlites and (more rarely) lamproites.

Cratons are restricted to areas of the world including South, Central, and West Africa, Canada, Brazil, Russia, India and Australia – all areas that produce or have produced diamonds.
Once recovered, rough diamonds are sorted by experts in a controlled, secure environment, and categorized or grouped into parcels for tender.

The rough diamonds are sorted into various parcels according to their shape, size, clarity and colour, and it is at this point that potential gem quality diamonds are separated from industrial diamonds. Industrial diamonds are lower-quality stones which are not suited for gem purposes, but are suitable for use in various none-gem related applications due to overall characteristics of diamonds (IE; drill bits, cutting tools, medical devices, etc).

Once sorted into appropriate packages, the diamonds are delivered to an accredited diamond bourse for tender in conjunction with various other producing mines goods. Tenders are typically held on a regular basis every four to six weeks depending on demand, and attended by the world’s diamond buyers who purchase goods on behalf of their clients, or for their own use.

Traditionally in the past, the majority of diamonds were sold through De Beers’ centralized selling channel, the Central Selling Organization (CSO), but it is now common for many companies, such as Suburban Minerals, to sell their rough diamonds to accredited diamond bourses and receive the best possible pricing.



Lota Bay (Bahia de Lota) Project
Lota Bay is located in the Gulf of Arauco, in the Municipality of Lota, Concepcion Province, Chile, South America. The project is a bituminous thermal coal deposit that lies on the seafloor to a depth of 10 meters and is directly adjacent to the shoreline of the bay, and is easily accessible by local industrial infrastructure, including a major dock and processing plant facilities. The concession is under exclusive option to Suburban Minerals, which has the right to acquire 100% of the project.

The resource, which sits on the harbor bottom, is there as a result of 145 years of dumping and spillage, in transit, of coal that was mined during the life of the nearby Lota coal mining operations, which were exhausted and shut down in the 1990’s. The initial reserve calculations in zone 1 of the concession are 275,000 proven, and 90,000 probable, tonnes of recoverable bituminous thermal coal having the following characteristics: 6700 Kcal/Kg, has less than 1% sulfur, and contains 14% ash.

Zone 1 of the concession encompasses 660,000 square meters of sea floor, where the coal rests in stratum, as well as two hectares of industrial land at the foot of the dock adjacent to the resource, where the land based coal preparation work will take place. All the necessary infrastructure is in place on the site; grid power, water, sewage disposal, highway and rail access, as well as a ready labor force from the nearby city of Lota, population 52,000.

The Lota Bay Coal Project has the support of the Chilean Government and the local community, which will benefit significantly from job creation as well as from environmental remediation and cleanup. Financial modeling shows conclusively that the recovery operation is economically viable and profitable at prevailing market coal prices and at the current proven resource level.



SUBB Key Company Management
Tim Sperling, President & CEO
Prior to joining Suburban Minerals Corp., Mr. Tim Sperling was the president of ENC Security from 2009 to 2012 where he secured important venture capital financing for the company as well as negotiate licensing agreements with several global clients. Mr. Sperling is a seasoned businessman with strong business development and negotiating skills.

Prior to becoming president of ENC, Mr. Sperling was a litigation lawyer from 1983 to 2008 when he retired from law. Mr. Sperling is a member of the State Bar of Arizona as well as a member of the Law Society of British Columbia. He holds a LLB and a BComm from the University of British Columbia.

SUBB Contact Info
SUBURBAN MINERALS CORP.
871 Coronado Center Drive
Suite 200
Henderson, NV 89052

Website: http://www.suburban-minerals.com/
Phone: 702-952-2817

tsperling@suburban-minerals.com
hr@suburban-minerals.com
info@susburban-minerals.com
ir@suburban-minerals.com

SUBB SEC Filings
http://www.otcmarkets.com/stock/SUBB/filings

SUBB Headlines
finance.yahoo.com/q/h?s=SUBB+Headlines

Investigate more about SUBB @ www.otcmarkets.com/stock/SUBB/quote for more due diligence.





Monday, February 24, 2014

$PROW - Progress Watch Corporation Due diligence

$PROW - Progress Watch Corporation DD



PROW Company Description
Progress Watch Corporation has been listed on the stock exchange since 1999 under the symbol PROW (OTCPink). It is an investment holding company previously focused on the mechanical movement manufacturing and watch supply businesses. The Company recently announced its plan to diversify into the mobile broadcasting technology market. Progress Watch Corporation is located in Senden, Germany.

PROW Products and Services
Quote:

Progress Watch Corp (PROW) Signs Letter of Intent with TeleDNA(TM) SENDEN, GERMANY -- (Marketwired) -- 02/04/14 Progress Watch Corp. (PINKSHEETS:PROW) has signed a letter of intent with TeleDNA. TeleDNA is at the forefront of global communications, providing products and innovations in IP and cloud networking; and wireless access to service providers throughout the world. TeleDNA is based in Bangalore, India.

For users of smartphones and devices on 4G/LTE networks, this means users will have new capabilities to stream and broadcast video. This technology streams feature-rich audio and video content instantly, without jeopardizing subscribers' privacy, or overloading the mobile network.

Progress Watch Corp. has selected TeleDNA to assist in the creation of a mobile network-based streaming broadcast technology. This technology is designed specifically to function on 4G and LTE mobile networks, and will provide significant capability in differentiation, segmentation, and revenue.

The TeleDNA team has collaborated with mobile network providers globally, and brings a diverse pool of experience in developing and implementing mobile technology solutions.
The Letter of Intent is the next major step in Progress Watch Corp.'s new direction into the mobile broadcast technology field.
http://www.stockwatch.com/News/Item.aspx?bid=U-i925714001-U%3aPROW-20140204&symbol=PROW®ion=U







Calibrum SA, 3250 Lyss, Switzerland:
Calibrum SA dedicates its strength to the development and production of high class innovative mechanical movements. Beside of different ongoing projects the prototyping stage of “START – see-through triple axe rotary tourbillon” has begun. This 3-axial tourbillon, patented by Progress Watch Corp. will allow to bring out such a product on the market for an interesting selling price, individualized as asked for by the watch brands.

The Calibrum "START" 
START is a triple axial tourbillon which indicates directly the time. The center cage is turning once in a minute and can indicate the second. The axes on which the Tourbillon is mounted rotates once in a hour and indicates directly the minutes. The whole tourbillon construction rotates furthermore once in 12 hours around the dial and indicates therefore the hours.

PROW Key Company Management
Board of Directors
Hans Handl, President . Appointed January 2009 (President as from February 2010)
Jan Wilgenhof, Secretary. Appointed July 2010
Anke David, Treasurer. Appointed January 2009



Mr. Hans Handl has been the President of Progress Watch Corporation since February 2010 and serves as its Chairman. Mr. Handl has been the Managing Director of Marburg Beheer B.V., since 1993. He has been the Managing Director of Nice Holding BV since 1998. Mr. Handl served as the Managing Director of Curam BV from 1973 to 1993. He has been a Member of the Supervisory Board at EIG European Investment Group AG as from 2003. Mr. Handl has been a Director of Progress Watch Corporation since January 2009. He serves as a Director of Calibrum SA.

PROW Contact Info
Progress Watch Corp.
Office United States of America
Progress Watch Corp.
375 N Stephanie St. 1411
89014-8909 Henderson, NV
USA

Representative Office Europe
Progress Watch Corp.
c/o Kley 27
48308 Senden
Germany
Phone: +49 (2509) 993690
Fax : +49 (2509) 9936919
info@progresswatch.eu
www.progresswatch.eu

website: http://www.progresswatch.eu/

PROW SEC Filings
http://www.otcmarkets.com/stock/PROW/filings

PROW Headlines
http://finance.yahoo.com/q/h?s=PROW+Headlines

Investigate more about PROW @ http://www.otcmarkets.com/stock/PROW/quote for more due diligence.

Sunday, February 23, 2014

$MDFI -Medefile International, Inc. Super Due Diligence

MDFI -Medefile International, Inc.



MDFI Company Description
Medefile International, Inc. is Headquartered in South Florida, MedeFile has developed and globally markets a proprietary, patient-centric, iPHR (Internet-enabled Personal Health Record) system for gathering, digitizing and organizing medical records so that individuals can have a comprehensive record of all of their medical visits.

MDFI Products and Services

Medefile - Why Medefile? Video http://vimeo.com/58826655


MedeFile's primary product is its web-based MedeFile solution, a highly secure system for gathering, maintaining, accessing and sharing personal medical records. Interoperable with most electronic medical record management systems marketed to the healthcare industry, the MedeFile solution is designed to gather all of its members' actual medical records and create a single, comprehensive Electronic Personal Health Record (ePHR) that is accessible 24 hours a day, seven days a week by the member and the member's authorized users on any web-enabled device (PC, cell phone, smartphone, e-reader) and portable MedeDrive unit.



MDFI Key Company Management
Ms. Niquana Noel has been the Chairwoman, Chief Executive Officer and President of of Medefile International, Inc. since January 28, 2014 and its Chief Operations Officer since August 12, 2013. Ms. Noel joined Medefile International as Operations Manager in 2008. Previously, Ms. Noel served as the Executive Assistant to a Florida-based serial entrepreneur who had successful business interests ranging from the ownership and operation of cemeteries in Maryland, Virginia and Florida; to the ownership and operation of exotic, high performance car dealerships and auto accessory businesses. Ms. Noel has been a Director of Medefile International, Inc. since August 12, 2013. Ms. Noel studied Business Management at Florida International University.

MDFI Contact Info
301 Yamato Road
Suite 1200
Boca Raton, FL 33431

Website: http://www.medefile.com
Phone: (561) 912-3393

MDFI SEC Filings
http://www.otcmarkets.com/stock/MDFI/filings

MDFI Headlines
http://finance.yahoo.com/q/h?s=MDFI+Headlines

Investigate more about MDFI @ http://www.otcmarkets.com/stock/MDFI/quote for more due diligence.




https://pennystockdivas.com/

Saturday, February 22, 2014

Light Media Holdings, Inc.~ LGMH Updated