Category Archives: Business of Medicine

Will the Catholic Church & the U.S. Courts Embrace Advanced Cell Technologies “Embryo-Safe” Technique Using Embryonic Stem Cells?

Advanced Cell Technology with laboratory facilities in Marlborough Massachusetts has pioneered a solution to the ethical, moral & legal debate raging in regards to protection of a human embryo. ACT has developed the “single-blastomere” technique. Patent Number 7,893,315 a non-destructive alternative for deriving human embryonic stem cell (hESC) lines.

This achievement in Regenerative medicine is a ground breaking feat for both Catholic and U.S. law.
• The 1995 encyclical The Gospel of Life, of which Pope John Paul II wrote: “Human embryos obtained in vitro are human beings and are subjects with rights; their dignity and right to life must be respected from the first moment of their existence. It is immoral to produce human embryos destined to be exploited as disposable ‘biological material'” (1,5 )
• The Dickey Amendment (also known as the Dickey-Wicker Amendment) is the name of an appropriation bill rider attached to a bill passed by United States Congress in 1995, and signed by former President Bill Clinton, which prohibits the Department of Health and Human Services (HHS) from using appropriated funds for the creation of human embryos for research purposes or for research in which human embryos are destroyed.

The single-blastomere technology uses a one-cell biopsy approach similar to pre-implantation genetic diagnosis (PGD), which is widely used in the in vitro fertilization (IVF) process and does not interfere with the embryo’s developmental potential. The stem cells generated using this approach are healthy, completely normal, and differentiate into all the cell types of the human The safety record for one-cell biopsy as part of PGD now has a 15-year track record, and is carried out routinely as part of IVF processes around the world. ACT’s technique of protecting the human embryo from harm can be expounded to the smallest blood transfusion in the world. As does a human being give millions of blood cells in a pint of blood so does ACT’s “single blastomere” process take but “one cell” from a 2 day old embryo. As the blood removed from a human donor “regenerate” the removed pint of blood so does the human embryo “regenerate” the one cell. Both of these procedures leave the human body & two day old embryo healthy. Both procedures are similar in that they both provide life saving material to those whom need them most to due to disease and other aliments of a medical nature.

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Global Health Progress Releases Non-Communicable Diseases Partnerships and Programs List

Global Health Progress compiled a list of non-communicable disease treatment programs from around the world, highlighting partnerships to address cancer treatment, diabetes care, epilepsy programs and more. The programs, sponsored by leading companies like Astra Zeneca, Abbott, Novo Nordisk, and Bayer Healthcare, aim to increase awareness of non-communicable diseases in the developing world.

“Our goal in creating this list is to bring awareness to these companies who work so hard at fighting diseases in developing countries,” explains Mark Grayson, Vice President of Communications and Public Affairs at PhRMA and key developer in the Global Health Progress initiative. “Non-communicable diseases are the leading killer in many of these countries, and without the help of these programs they would continue to increase.”

Global Health Progress works with partner groups to encourage and sustain funding for the research and development of healthcare in developing nations. Improving health care systems and access to medicines, especially in the developing world, requires multifaceted approaches and solutions. Research-based biopharmaceutical companies are active partners in some of the largest and boldest health initiatives that explore new and effective ways to provide treatment, care and education to millions of people in developing countries.

Read the full list of non-communicable disease treatment programs here:
http://globalhealthprogress.org/mediacenter/wp-content/uploads/NCD-Health-Partnerships-and-Programs_Worldwide-05-02-11.pdf.

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Side by side comparison of Advanced Cell Technology & Geron Corporation

Regenerative medicine is a highly complicated and vastly misunderstood science. Investor Stem Cell is dedicated to bringing investors and stakeholders together in thoughtful discussion to educate and publicize the incredible advancements unfolding in the regenerative medicine sector. A quantum leap in health care is upon the world. Will you profit from this emerging sector & help bring cures to millions? Find out now what the street thinks at www.investorstemcell.com.

Side by side comparison of Advanced Cell Technology & Geron Corporation:

Geron Corporation (NASDAQ:GERN), Approved by the FDA to use human embryonic stem cell (hESC) treatments to treat spinal cord injuries. The research Goliath is a well-funded machine employing the top minds in the world working on everything from mid-stage oncology trials to promising (hESC) drugs for spinal cord injuries, heart disease & cancer.

Snap shot of Goliath: Geron Corpoartion-(NASDAQ:GERN)-
• Seven oncology Phase 2 trials currently underway, and has several big Pharma joint venture agreements in oncology animal and human trials
• Five hESC areas of investigation underway. GRNOPC1 is the lead candidate. Geron destroys the human embryo through its (hESC) R&D, of which the company uses the blastocyst embryo formation at day five after fertilization from IVF clinics
• Cash, restricted cash, cash equivalents and marketable securities: $221,274.000.00
• Total operating expenses in 2010: $114,730,000.00
• 175 employees; over 100 hold PhD or MD degrees
• Geron Corporation was founded in 1990 and is based in Menlo Park, California
• Trades on the NASDAQ providing liquidity & large institutional investors
• Corporate financial statements:http://www.geron.com/investors/reports/GeronAnnualReport2010.pdf

Advanced Cell Technology not too long ago was the predominant leader in the field of regenerative medicine. It fell from that distinction in part due to executive management hubris and ultimately the credit crisis in mid-2008. ACT was able to resurrect itself from near bankruptcy in June 2008 and now has the distinction of holding two out of the three FDA approved (hESC) trials. ACT is led by a competent executive management team and employs several of the most predominant regenerative researcher(s) in the world.

Snap shot of David: Advanced Cell Technology-(OTC:ACTC)-
• Retinal Pigment Epithelial Cell Program is their lead program-(HESC) trials for both SMD/AMD are expected to start in week(s) Jules Stein Eye Institute at the University of California, Los Angeles (UCLA ) will conduct the 2 (hESC) trials for Stargardt’s Macular Dystrophy (SMD) and Dry Age-Related Macular Degeneration (AMD)
• Filed a European Clinical Trial Application for Phase 1/2 study using (hESC) to treat macular degeneration
• Issued a broad patent for hESC-derived RPE cells in China
• Seeking funding & joint venture partner for Myoblast program for the treatment of cardiovascular disease Phase 2 approved by the FDA
• Joint ventured with Korean medical giant CHA to form “Stem Cell & Regenerative Medicine International” (SCRMI). This partnership expected to file an investigational new drug application (IND) with the FDA in Q-4 of this year. CHA biotech is waiting for final approval from the Korea Food and Drug Administration for (hESC) trial for AMD
• Issued patent on its “single-blastomere” technique. Patent Number 7,893,315 broadly covers ACT’s proprietary single-blastomere technology that provides a non-destructive alternative for deriving hESC lines. This “Embryo-Safe” one-cell biopsy approach similar to pre-implantation genetic diagnosis (PGD), which is widely used in the in vitro fertilization (IVF) process and does not interfere with the embryo’s developmental potential
• 22 full-time employees, six hold PhD or MD degrees-Formed in 1994, HQ in Menlo Park, California with laboratory facilities in Marlborough, MA
• Total operating expenses in 2010: $22,044,701
• Cash, restricted cash, cash equivalents and marketable securities: $34,889,409
• Trades on the OTC:BB ACTC is a Sarbanes–Oxley Act SEC reporter
• Corporate financial statements: http://www.sec.gov/Archives/edgar/data/11...

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From Universal HIV Testing to HIV Cure

People involved in the fight against HIV/AIDS will gather in Marseille, France, May 23-25, 2012 for an international AIDS Conference under the theme: ‘From Universal HIV Testing to HIV Cure’.

The ISHEID (International Symposium on HIV & Emerging Infectious Diseases) is a major scientific event attracting doctors, biologists, researchers, patients’ representatives and policy makers from all around the world. Its next edition, to be held just more than one year ahead, will focus on recent developments against this pandemic.

Despite major advances in antiretroviral therapy, HIV still infects daily 2,000 new individuals and kills 2 millions each year. Current treatments are life-long with problems of compliance, resistance, toxicity, access, and cost.

‘There are advances both in the area of prevention, testing and potential cure’ told Alain Lafeuillade, a French Doctor involved in the organization of the conference. ‘Our driving force is to draw to the conference the best experts in the world for each program theme’. Antiretroviral treatment as prevention (or pre-exposure prophylaxis) will be debated with the pros and cons. Human rights and access to HIV care will be the focus of en entire session. Current issues in antiretroviral therapy management will be discussed during 2 sessions. Finally, the best American experts in the field of HIV reservoirs and eradication research will present their latest discoveries in the search for a cure.

The international Steering Committee will actively build a program the most exciting possible in the forthcoming months. Meanwhile, interviews of renowned experts are regularly published on the meeting website: http://www.isheid.com/en/committees/interview.html

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New Website Dedicated To Stem Cell Investors

Investor Stem Cell (http://www.investorstemcell.com) is dedicated to bringing investors and stakeholders together in thoughtful discussion to educate and publicize the incredible medical advancements taking place in the regenerative medicine sector. Scientists are using stem cells both (hESC) and (iPSC) in hopes of easing the suffering of hundreds of millions of people world wide.

Our society is on the verge of a quantum leap moment in time thanks to regenerative medicine.

Regenerative medicine and Stem Cell research:

Utter those words at your next dinner party or casual gathering of friends and family. You will receive a concoction of half-truth’s and out right fallacy responses. Stem Cell research conjures images of futuristic Star–Trek like preservation chambers, human looking ears protruding oddly from the backs of mice, or worse yet an image of a late term fetus. Nothing could be farther from the truth when entering the reality of Regenerative medicine.

Never before has this area of research been more exciting and promising than right now. There is a medical revolution brewing, and like any revolution, there are those who want to suppress this uprising for continued personal and ideological gains. If we were to take all the major advances in the past 500 years of human medical history and multiply its effect by 10 fold it still would not compare to the paradigm shift in health care delivery that the world may witness in this decade using stem cells. Imagine that an $800,000 heart transplant is no longer needed and that instead the same money spent on one patient can now be stretched out to treat 20 patients who are needing a heart transplant. Is this what Regenerative medicine has in the offing? Only time will tell. Our healthcare system could very well be on the verge of a quantum leap moment thanks to regenerative medicine.

The Food and Drug Administration (FDA) authorized 3 trials using human embryonic stem cells (hESC) in late 2010. Validation of hESC research efforts and the culmination of billions spent on research are coming to fruition. FDA validation for the treatments of spinal cord injury and age related macular degeneration is expected in 2011. It may be the shot heard around the world event sometime in late Q-4 2011 for the Regenerative medicine sector.

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Medelita medical coats feature state of the art fabrics and durable design features

Medelita®, maker of breakthrough performance medical coats for both men and women, offers the best selection for those medical professionals who are looking for functional, professional appearing coats. Featuring state of the art materials and smart, flattering designs, Medelita continues to push above and beyond the competition in order to offer medical professionals the very best quality and selection in the medical uniform market.

Medelita medical coats are made from pre-shrunk, 100% cotton textured fabric, which allow for a soft, sophisticated finish that is immediately noticeable. While most medical coats are unisex in styling, Medelita coats are contoured gender specifically for men and women, creating a durable and functional fitting garment that remains comfortable throughout the work day. The overall dimensions and styling of the medical coats are specifically designed to allow for ample forward reach without limiting range of motion in the arms, shoulders, or neck. In addition, Medelita coats also offer modern features like women’s rounded lapels and men’s blazer chest pockets.

As medical professionals wear medical coats in high pressure, stressful situations, Medelita medical coats use breathable 100% cotton fabric that features High-IQ Easy Care Plus wrinkle resistance and Advanced Dual Action Teflon fabric stain protector, the latter of which allows fluids to simply run right off the fabric.

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Medelita partners with the Society for Dermatology Physician Assistants

Medelita®, maker of breakthrough performance lab coats for both men and women, announces a new partnership with the Society of Dermatology Physician Assistants. Member benefit discount and affiliation agreement begin on May 1st.

The Society of Dermatology Physician Assistants is a non-profit professional organization comprised of individuals who provide dermatologic care, or have expressed interest in the field of dermatology. The SDPA organization, founded in 1994, has over 1,700 members and continues to grow. The main focus of the organization is to provide continuing medical education to its members, form leadership structure, act as an advocate for members, and develop resources for the evaluation and hiring of Physician Assistants. Medelita is proud to have this affiliation with such a prestigious PA organization, as the founder is also a PA. The partnership is extremely complimentary.

Dermatology PAs find Medelita lab coats to be especially professional and classy, with a comfortable, ergonomic fit. With a fit similar to professional clothing, and styling and workmanship improvements throughout, doing procedures from multiple angles and positions is now easier and more comfortable. Coupled with the Advanced Dual Action Teflon® fabric protector, the performance of the lab coats is ideal for those clinicians who are at higher risk for exposure to bodily fluids or other spills. Medelita high-performance lab coats help to ensure a clean, bright white appearance by preventing soil and stains from setting in, and also allowing a fluid barrier.  They wash better than any other lab coat available, and stay bright white.

“We recently received a testimonial from a dermatology PA who said that on the very first day that she received her Medelita lab coat, blood splashed onto the sleeve during a procedure,” shares Lara Manchik, PA-C and founder. “She simply “brushed” it off with a hand towel – with no trace of it left on the surface.  Her supervising MD immediately asked where he could get a similar coat of the same performance quality.”

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Medelita Gives Back With Newest Affiliation

Medelita®, lab coat manufacturer and online retailer upscale men’s and women’s medical apparel, is pleased to announce their latest affiliation with the American Academy of Cosmetic Dentistry. Currently AACD members who make purchases through Medelita.com receive a 10% discount. In addition to this member discount, the premier lab coat and medical scrubs retailer will donate 5% off every purchase to the Give Back a Smile Program.

The AACD is dedicated to advancing excellence in cosmetic dentistry and encouraging high standards in patient care. The American Academy of Cosmetic Dentistry Charitable Foundation’s (AACDCF) mission is to assist in rebuilding the lives and dignity of survivors of domestic violence through compassionate cosmetic dental services and support programs. Our program provides restorative and cosmetic dentistry in the smile zone at no cost to qualified survivors through our nationwide network of volunteer cosmetic dentists and our support team of laboratories and dental manufacturers. Similarly, Medelita also holds elevated standards in providing professional, sophisticated, technically advanced apparel to the dentists, physicians, and surgeons they serve. Thus, the affiliation is a synergistic fit.

AACD members are able to choose from four dental-specific lab coats, or from seven additional lab coats and multiple colors of men’s and women’s scrubs, all visible at www.medelita.com. In addition to lab coats and scrubs, Medelita offers the very best clogs available to healthcare professionals. Medelita not only provides the essentials, but specifically designs dental-specific lab coats with cuffed sleeves and optional closure to the neck. By following OSHA recommendations for garment construction, and combining those features with quality construction and Advanced Dual Action Teflon® performance fabric, members appreciate Medelita as a thoughtful uniform ideal for dentists.

Members of the AACD will receive a 10% discount on all purchases made through Medelita by entering the promotional code GBSMILE. In addition, with every purchase made, Medelita will donate 5% to the Give Back a Smile Program. This program founded by the AACD was developed in recongnition of addressing the needs in the communities of AACD members. Volunteer cosmetic dentists and laboratory technicians agree to restore the broken and damaged teeth of survivors of intimate partner violence at no cost. More than 1,000 U.S applicants have received services from this program.

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Medelita Providing In-House Embroidery Services

Medelita®, breakthrough performance maker in medical scrubs and lab coats for both men and women, announces that all embroidery services are now completed in-house. With two top-of-the-line embroidery machines and an expert embroidery team, the premier medical apparel retailer is able to provide high quality customization without the need to outsource.

Medelita, known for their superior quality physician scrubs and performance lab coats has always offered custom embroidery services for their clients. Previously outsourced, resulting in lengthy lead times and frustrating delays, customers can now opt for Medelita in-house customization options and experience less than 10 day completion on any lab coat or medical scrub top embroidery order. Embroidery is completed by artisans with complex digitization experience, resulting in the very best quality logo and name & title stitching in the medical apparel industry. Custom options include name & title embroidery up to 3 lines, professional organization logo embroidery, and custom logo design for private practices, hospitals or university settings.

The fine quality and careful precision that goes into every stitch is consistent with the high standards that Medelita maintains on their lab coats and scrubs. Founder Lara Manchik, PA-C, states “Embroidery is the closest thing to wearing your diploma. For that reason it must be perfectly displayed, as a symbol of prestige and aptitude.”

With lab coat embroidery prominently displayed as acknowledgement of one’s educational achievements, physicians and surgeons can feel distinguished and elegant with professional embroidery from Medelita.

By conducting all embroidery services in-house, Medelita can ensure that the finished product is met to their high standards. All embroidered items go through a triple-check process that boasts an error rate of less than 0.01%. No other medical apparel company performs all these types of services strictly in-house, nor with such high standards or resultant quality.

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Housing Market Crash and Rising Medical Costs, Is There A Connection?

As millions of American homeowners know, the housing market crash was fueled by inflated home values and bank loans that were high above the equity or actual value of “underwater” homes. According to Trisha Lotzer, JD., health-care attorney and CEO of Physis, Inc., a similar threat for banks, borrowers and owners of many of the nation’s medical, dental, optometry and veterinary practices must be averted.

Like residential real estate, medical practices may be marketed and sold by brokers. Brokers in the business of selling medical practices commonly charge 7-12% commission. The commission alone can add $80,000 to $2,000,000 to the purchase price, depending on the size of the facility–and drive up the bank note accordingly.

Like real estate agents, the job of the practice broker is to get the seller the highest selling price possible. Unlike real estate agents, however, brokers are often the only ones who value the practices they have for sale–giving them a built in incentive to inflate the value of practices and increase their commission. Ross Landreth, MBA, explains that the problem occurs when a practice is arbitrarily valued, purchased and financed at $1,500,000, but only has an actual fair market value (per USPAP approved valuation standards) of $850,000. This could mean that the practice does not cash-flow at $1,500,00 and that the new purchasers would have to raise the price of services in order to maintain profitability and pay back the bank note. This increase in the cost of health care does not increase the earnings of the practice owners or physicians but is passed along to patients and insurance providers.

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Medical Innovation Protection Stressed in EU-India Free Trade Agreement Talks

The Financial Express published an article on the Free Trade Agreement (FTA) talks that continue between the European Union (EU) and India. One of the most discussed and disagreed upon parts of the proposed FTA involves the need for protecting the intellectual property of pharmaceutical companies in order to promote medical innovation and investment in the development of new medicines and research. This disagreement about whether data exclusivity in the pharmaceutical sector should be included has resulted in the delay of finalizing the FTA.

Pharmaceutical companies rely on data exclusivity to protect the investment made in developing the medication that is used throughout the world. Millions of dollars are spent on clinical trials to prove the safety and effectiveness of these drugs. These exclusive rights prevent competitors from obtaining marketing licenses for lower cost versions of these drugs.

Global Health Progress (GHP) is committed to being part of the effort to create a sustainable health care system that includes improving access to health care and continuing medical innovation and progress for all people. While the pharma industry is divided on the issue, GHP supports efforts to improve regulations protecting pharmaceutical companies’ intellectual property. Without this protection, the funding of studies that bring these medications to market could suffer.

Improving health care systems and access to medicines, especially in the developing world, requires multifaceted approaches and solutions. Research-based biopharmaceutical companies are active partners in some of the largest and boldest health initiatives that explore new and effective ways to provide treatment, care and education to millions of people in developing countries.

About Global Health Progress:
Global Health Progress also supports efforts to raise awareness and mobilize resources to address health challenges in the developing world by bringing local leaders together with international health experts, policymakers, donor governments, and the private sector.

www.globalhealthprogress.org;

twitter.com/globalhealth;

facebook.com/pages/Global-Health-Progress/124850684219049;

linkedin.com/groups?home=&gid=2972068

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Global Health Progress Amplifies Report Calling for Funding Products to Fight Neglected Tropical Diseases

The third-annual Global Funding of Innovation for Neglected Diseases (G-FINDER) survey was released last week revealing both good and bad news for the funding of neglected diseases in the developing world. In a press release issued by Policy Cures, an independent group providing research and analysis for those involved in the creation of new pharmaceuticals for neglected diseases, the group reveals that while funding for neglected diseases has increased, funding for new products has decreased.

Funders appear to be focusing more of their money toward traditional basic research. This shift has caused a $50 million drop in funding for Product Development Partnerships (PDP), non-profit organizations that partner with external organizations to drive product development for neglected diseases, including neglected tropical diseases.

Report author Dr Mary Moran, Director of Policy Cures warns funders not to “take their eyes off the ball” in the press release, stating that while the increase in funding is encouraging it is important that the funds are spent wisely.

Global Health Progress has worked with partner groups to encourage and sustain funding for the research and development of new products. The innovative research and development (R&D) of new drugs and vaccines is a critical component of improving health care and combating epidemics of neglected tropical diseases in developing countries. There are no vaccines or cures for some widespread and life threatening diseases such as malaria, while existing treatments for diseases such as tuberculosis are becoming less effective due to drug resistance.

Read the full press release from Policy Cures here:
http://globalhealthprogress.org/mediacenter/wp-content/uploads/G-FINDER_Year_3_media_release.pdf,
or read the G-FINDER report on the Policy Cures website:
http://www.policycures.org/downloads/g-finder_2010.pdf.

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Big Mountain Pharmacy Launches a New Blog: Blogging the Drugs

One thing that has often been lacking from online Canadian pharmacies is information. Not only about the drugs on sale themselves, but also about illnesses and general news on the medical industry such as regulation and equipment.

That is what triggered Big Mountain Drugs to start their health information blog, which is now fully up and running on their website offering articles packed with information about common illnesses such as Alzheimer’s, erectile dysfunction (impotence) and acne. Not only that, they have also released articles giving useful information to help with particularly common issues. These include helping patients with poor eyesight by giving tips on how to identify medication safely, and giving family and friends of patients’ advice on how to tell the difference between dementia and depression.

Information like this is extremely valuable to patients, as they can learn more about the drugs that they are taking and the conditions that they are taking them for. The knowledge to patients increases safety as they can easily spot the symptoms of complex or potentially dangerous illnesses, and learn how to deal with the issues that come with many conditions. Blogging the Drugs from Big Mountain pharmacy, which can be found on their website, now lists many informative articles to help their customers. All of the information is free, and is written by medical professionals giving accurate and interesting information and facts.

One customer said: “Blogging the Drugs from Big Mountain pharmacy is extremely helpful and I’ve discovered a lot of new things about my illness that I didn’t know before, including information about the drugs that I am taking so that I can keep an eye out for side effects. It makes me feel much safer that I have more knowledge than I did before”.

Big Mountain Drugs commented “We wanted to add value to our customers by allowing them to make more informed decisions. Although they cannot buy most of the drugs without a prescription, it still gives them the opportunity to learn about the drugs that they are prescribed by their doctor so that they can speak with their doctor if they have any concerns. It also helps them to learn about their illnesses so that they can be aware of any issues such as symptoms of their conditions”.

One concern however, is that online Canadian pharmacies as of recent times, are no longer allowed to advertise on Google unless it is in their own country, which will mean that many people searching for information on drugs online will not be able to find the blog unless they live in Canada if they use Google to search for it.

You can join the blog on Facebook (bigmountaindrugs) and Twitter (bigmountaindrug), some of the most popular social networking sites so it is always very easy to connect and check out any new information that is issued by Big Mountain Drugs. They also post videos on Youtube and you can subscribe by RSS feed so that you get information in new articles as soon as they are posted online.

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Global Health Progress Encourages Global Partnerships on Access to Health Care

Starting this month, members of Congress will be looking closely at U.S. spending as they work with the White House to build the 2012 budget. One area that has come under increased scrutiny is U.S. spending on global health programs. Several groups last week announced a petition (http://www.supportglobalhealth.org/) seeking support for global health spending through the United States Global Health Initiative. Many fear that even flat spending in this area could jeopardize important programs in vaccine research and treatment.

News like this highlights the important role that public-private partnerships play in supporting access to global health care. The Global Health Progress initiative seeks to bring research-based biopharmaceutical companies and global health leaders together to improve access to medicine and health care in the developing world. We are committed to being part of the effort to create a sustainable health care system that includes improving access to health care and continuing medical innovation and progress for all people.

Research-based biopharmaceutical companies and their partners around the world are working to implement sustainable solutions and strengthen the health care delivery systems so they can meet tomorrow’s challenges. Millions of people lack access to essential medicines due to factors including incomplete delivery systems, lack of training for health personnel, lack of infrastructure and the cost of treatments. We must address the underlying barriers to health care, such as weak and fragmented health systems, limited health care personnel and inadequate resources for scaling up proven solutions. The innovative research and development (R&D) of new drugs and vaccines is a critical component of improving health care and combating epidemics in developing countries.

Through meaningful public-private partnerships with others in the field, including policymakers in the developed and developing world, multi-lateral institutions, non-governmental organizations, and academia we can help shape sustainable solutions that improve the health of all people.

To stay informed on the latest news about global investment in pharmaceutical R&D and improving access to medicines, sign up to receive special alerts and newsletters. You can also spread the word about the efforts of the Global Health Progress initiative and keep others informed about how we’re affecting change around the world, or share your story about how you or someone you know is working to promote global health.

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White Collar Uniform Introduces our New Women’s Lab Coat Collection

White Collar Uniform®, makers of the all new prestigious women’s lab coats is having their Grand Opening this month at our new exiting website online. White Collar Uniform’s clothing has been described as breakthrough clothing for men and women doctors and physicians in the medical field. White Collar clothing has been described by many medical professionals as being practical and having overwhelming beauty and style.

Our women and men lab coats are very upscale clothing for doctors and we have a very creative designing team working around the clock to make you look good. White Collar has invented the first every lab coat that can interact with the wearer by helping the doctor to hold their tools while in the consultation room and on the floor. This lab coat is spectacular says one doctor who happened to see our lab coats for the first time. We have created the best looking lab coat in the world and nobody can make claims against that!

White Collar Uniform’s top of the line lab coats can be purchased for under $50.00, which is more than a 45% savings from our standard price. White Collar Uniforms is the low price leader and we will not be undersold by anybody looking to take our place. Our top of the line lab coats are loaded with goodies that the doctors are going to really enjoy. Just take a look at our lab coats on any picture and you will see that we are the best looking coats out there – hands down!

Attention: There has been a lot of recent articles talking about lab coats and transmitting bacteria via through lab coats. Most doctors hang on to their lab coats for ages until they finally have to throw it away. We recommend that you change your lab coat every six months. There has been a lot of talk about soil proof coats and treated fabrics, “Don’t be too quick to get on this band-wagon!” Studies have show that these clothing can not be autoclaved so be careful about their labeling in general.

Don’t spend a lot of money on scrubs and lab coats that won’t hold up to the test of time. These so-called treated clothing’s are very expensive and they will probably send you running to the bank for cover. If it doesn’t say white collar, “Then it must be blue!” Save yourself a bundle and shop for White Collar Uniforms when you decide to purchase your next order of lab coats or scrubs online. Also you should watch out for repellant type materials which makes claims that doesn’t make sense most of the time.

White Collar Uniforms was founded several years ago by a well known inventor and medical provider in the medical field. He wanted to design a men’s lab coat for men and women that could let them use their hands more and be more practical at the same time. Since then, he has consulted hundreds and thousands of his constituents and his final works have been published amongst his peers and medical friends. Doctors deserve better and that’s why White Collar Uniforms invented its sporty designer lab coats.

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Assay-Ready Chemistry Partnership between Molplex & Enamine

Molplex and Enamine today announced a new partnership to offer the Enamine screening collection of 1.8 million stock chemicals through the Molplex online drug design and assay-ready chemical supply services. The agreement is a major step towards eliminating the high start-up costs ofdrug discovery, bringing sophisticated drug design, compound management and assay-ready chemistry to the world’s drug discovery scientists on demand.

The agreement adds Molplex online drug design systems to the deep experience in organic chemistry and compound management of Enamine to solve the problem of generating viable chemical leads for novel targets.

Molplex CEO David E. Leahy said: “We are very proud to be selected by Enamine as their partner for on demand drug discovery services at a time when major restructuring of the industry is creating new opportunities and new markets for our combined expertise. This agreement marks a step change in the size and scope of our assay-ready chemical supply service and major progress towards our goal of being the world’s first choice partner for enabling the long tail of drug discovery”

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Gene Therapy and Stem Cell Therapy Standard Developed For A Unique Derivative Of Post Hetero-Plastic Inplantation Chronic Inflammation Syndrome, The NIDO Disease

Researchers task force, led by faculties of T-Protocol, registered Genom Project as controlled genom project in the hosted database of NCBI, a publication matter authority and function assigned organization under oversee of Department of Health & Human Services, reached once to share the exegetical impression officially pre-published concerning the understanding specific spectrum of symptoms covering boroad range of character usually complained and observed through chronic inflammation, granuloma, some types of lymphoma and various uncommon symptoms to let physician scientists suspecting indicium of neurological diseases, NIDO disease, an unique type of post hetero-plastic implantation chronic inflammation syndrome and setting Massachusetts indications of treatments standardized manual (Massachusetts manual) & diagnostic and standardized medical treatment manual for post hetero-plastic inplantation chronic inflammation syndrome, specific edition against NIDO Disease.

The once defined causes of NIDO disease, an unique type of post hetero-plastic implantation chronic inflammation syndrome are considered each of a common living organism to cause conformational diseases like Creutzfeldt-Jakob disease, Alzheimer’s disease, Parkinson’s disease, Huntington’s disease and kinds of and a set of biochemical and physical reaction and response realized by cross-species gene- mutation, as biotransformation, easily describing natural physiological and biochemical changes in vivo substrate of human bodies. After this studies, standardized protocol of gene therapy and applied stem cell therapy is now in practice and on available.

Faculties,committing themselves entirely to the project, of each institutes and organizations participating the project to ascertain proteins and DNA/genomic DNA/genom of human, other mammal and virulent microorganism including bacillus/virus affecting each symptom and the symptoms’ spectrum expressed generally and observed commonly on patients suffered from NIDO disease, extraordinarily unique derived type of post hetero-plastic implantation chronic inflammation syndrome and to develop diagnostic standard and treatment protocol standardized and to find a clue compose gene therapy protocol and applied stem cell therapy protocol to entirely heal NIDO disease, an unique type of post hetero-plastic implantation chronic inflammation syndrome and to let all of current suffered patients from various combined symptoms directly derived by chronic inflammation and various tumors, have to express full surprise at the fact that these disease and patients suffered are made up and left no attention and no relief.

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New UN Program Will Ensure Developing Nations Continue to Have Access to Drugs Effective At Treating Malaria

Earlier this week, the United Nations announced a new plan of action designed to help fight disease resistance to artemisinin, the world’s most potent treatment for malaria. Launched by the UN World Health Organization (WHO) and the Roll Back Malaria Partnership (RBM), the groups hope to better contain and prevent resistance to artemisinins, the critical component of artemisinin-based combination therapies (ACTs), which are currently the most effective weapon in treating falciparum malaria.

The WHO’s announcement describes the plan as a five-step process which “aims to contain and prevent artemisinin resistance by stopping the spread of resistant parasites, increase monitoring and surveillance for artemisinin resistance, improve access to malaria diagnostic testing and rational treatment with ACTs, invest in artemisinin resistance-related research, and motivate action and mobilize resources.”

Global Health Progress is hopeful that this action plan will help to ensure that developing nations continue to have access to drugs that most effectively treat malaria. Many malaria-stricken countries lack the resources needed to keep an effective health care system running smoothly. Strong, effective health systems are vital to helping those in need of access to drugs, and health care improvements made today will strengthen the ability of countries to develop sustainable systems that can meet tomorrow’s challenges. Stopping the spread of drug-resistant strains of malaria and other diseases are essential to these goals.

Investing in local R&D capacity and national research systems is another way research-based biopharmaceutical companies help strengthen health systems. Local production can play a valuable role in building overall local capacity and enabling developing countries to increase access to essential medicines.

It is the responsibility of the entire international community to facilitate access to medicines. Success depends on all sectors working in partnership; not only to make medicines more accessible, but also to ensure continued innovation into new medicines for the treatment and prevention of all diseases.

About Global Health Progress:
Global Health Progress also supports efforts to raise awareness and mobilize resources to address health challenges in the developing world by bringing local leaders together with international health experts, policymakers, donor governments, and the private sector. www.globalhealthprogress.org;  twitter.com/globalhealth; facebook.com/pages/Global-Health-Progress/124850684219049;  linkedin.com/groups?home=&gid=2972068

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Next Genetic Natural Stem Cell Therapy Established

Division of Gene Medicine & Stem Cell Application, School of Medical Science, complete the research and established completely new protocol totally recovering natural bio mechanism of hair regrowth.

The researchers, led by Lord. Prof. Dr. Daichent Otto Rie, specified protein and genom to affect internal bio mechanism to generate hair and control the level of successful growth being low which is the baldness.

The key cast of the set of the bio cycle is hair follicles, which is stem cell on head skin and effect or holding function to cure many neurotic diseases and disorders like Alzheimer’s disease – Prion Disease and even Trion Disease (Post Hetero-Plastic Implantation Chronic Inflammation Syndrome; PhCIS) has absolutely unique character being retrieved absolute stem cell, which can recover the ability as stem cell after got adult. The key genom and DNA has been found through the Genom Project’s T-Protocol research developing in the government registered Genom Project since 2005. The most concentrated attention of researchers is not “what is cause” but “What protocol is best”.

The team of Prof.Daichent has successfully completed in vivo and in vivro experiment actually using voluntary patients whose types of hair loss being across over highly wide range extent to even lymphoma and cancer and finally established next genetic hair loss curing treatment protocol mainly composed of stem cell therapy and gene therapy.

Most of cases are treatable through entry level stem cell theraputic technique or HIV-1 Vector using high level technique but A20 introduction as gene therapy is required when treating patients being suffered from lymphoma, cancer or any neurotic diseases like Alzheimer’s disease – Prion Disease and even Trion Disease (Post Hetero-Plastic Implantation Chronic Inflammation Syndrome; PhCIS).

As Prof.Daichent points since 2005 being on School of Public Health of Harvard, in the treatment manual (published 2005), the key factor to overcome of lymphoma and chronic inflammation on human skin is extraordinary redundancy coding of polyglutamine DNA synthesis as the type of disease caused by pathological proteins and lack or heavy impairment of an specific DNA of A20.

Actually, the treatment protocol curing for baldness is also found through T-protocol which was essentially aimed at achieving causal and complete treatment of lymphoma, cancer, chronic inflammation and many neurotic diseases.

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ClinACE Initiates Global Clinical Research Awareness Day

The world and the new millennium stands witness to revolutionary breakthroughs happening in the medical research arena. New drug or botanical discoveries and therapies that will perhaps cure life threatening diseases and bring about improved quality of life – is the order of the day.

All this and more, possible due to endless and tireless work in the area of Research and Development by organizations united on one single front. To meet unending medical demand and necessities and make effective healthcare more accessible to the population at large.

Research on humans to harness the goodness of potential drugs has been carried out since centuries. Human Trials are a definitive and most important link in the process of Discovery to Development and Commercialization. However, tales of unethical and almost inhuman conduct related to these trials with little or no protection of subject rights have been etched in history and in the minds of many.

The beginning of every change is awareness. A new idea, thought ingrained to bring about a difference is worthy of its cause. Human Trials since long have been a topic of prejudice and of concern to a few. Are they safe? Are they necessary? And many more such queries would always remain in ‘a valley of doubt’ if not answered or addressed accurately.

‘Global Clinical Research Awareness Day’ – An initiative by ClinACE to bring to light the ethical framework of Clinical Research which has undergone an evolution from negative perception, injustice, and manipulation of subject rights to bringing safe, effective and quality healthcare without compromise. It is our endeavor to spread the good word about Clinical Research and Protection of Subject Rights.

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