Economic constraints impact pharmaceutical development and supply

With the downturn in the world economy already putting the pharmaceutical industry under pressure, an increasingly small number of novel products are coming to market. The innovation capacity of the pharmaceutical industry is determined, to a great extent, by the external environment. Consequently, pharmaceutical innovation is likely to suffer, partly due to increasing government barriers precluding access to reimbursement lists. Furthermore, as governments push for greater use of generic drugs, the pressure on big pharmaceutical companies and their ability to be innovative will increase.

 

Cost-effectiveness and safety of a product are at the top of the agenda for payers. Global healthcare costs are rising due to ageing populations and poor lifestyle choices - particularly in western markets. Consequently, governments and payers across the seven major markets are implementing numerous healthcare cost-containment policies.

 

The US system of funding healthcare, which is generally seen as spending lavishly by international standards, has also become more cost conscious due to rising healthcare costs, which in turn are driving up insurance premiums. Insurance firms are beginning to seek better deals on prescription drugs from pharmaceutical companies in order to avoid raising insurance premiums further in a country that is in an economic recession.

 

For those patients in the US that do not have the means to afford medical insurance, a pilot scheme (introduced by the FDA in 1988) exists, whereby patients can order up to three months supply of medication by providing a registered pharmaceutical supplier with a valid prescription. More details of the service that Masters provides can be found in the ‘Customer’ page of our website.

 
Counterfeit medicines and bogus pharmacies on the increase

Brand protection firm MarkMonitor has released its latest "Brandjacking Index," a study that tracks the online presence of six major drugs to determine if the products are being sold by unreputable pharmacies, used in unsolicited spam e-mail, or being counterfeited outright.


The results show that in June 2008, more than 20,000 websites abused drug trademarks. Included in the figures were 2,986 suspicious online pharmacies delivering 60 million spam e-mail. Although the six drugs have not named, they are thought to include a lifestyle drug, a sleep aid, anti-cholesterol, and an ulcer medication.


The biggest increase, year on year, is an 87 percent boost in offensive content on sites that are marketing pharmaceuticals. More concerning is a 66 percent spike in e-commerce sites marketing pharmaceuticals, which jumped from 3,052 in the second-quarter of 2007 to 5,070 in the same period this year.


While the number of bogus online pharmacies is growing, so is the traffic at the sites and the deep discounts being offered. It was also noted that these sites are engaging in paid advertisement to draw consumers.


Masters is recognized as a registered pharmacy with the Royal Pharmaceutical Society of Great Britain, and by the Florida State Department of Health.

 
Masters approved as a registered pharmacy by RPSGB

Masters has been registered on the accredited pharmacy list by the Royal Pharmaceutical Society of Great Britain (RPSGB). The voluntary scheme has been set up to ensure that the public can easily distinguish a safe and legitimate website to buy from.

 

The accompanying logo displays the pharmacy's individual registration number. When the logo is clicked on, it directs the user to the RPSGB website, confirming the pharmacy's registration details.

 

 

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FDA encourages development of tropical disease drugs

The United States is set to launch a prize system to encourage pharmaceutical companies to develop drugs for tropical diseases. Sixteen tropical diseases, including sleeping sickness, leprosy and malaria are listed as eligible for the scheme.

 

Under the system, companies producing a drug or vaccine for a tropical disease can apply for a Priority Review voucher, which allows them a shorter approval time for another drug at a later date.

The shorter approval process would take approximately six months instead of ten, meaning that drugs could hit the market sooner and potentially be more lucrative. Thus, the vouchers are estimated to be worth around US$300 million.

 

Companies can also take advantage of the Orphan Drugs Act, under which drug developers receive tax credits, a waiver of the US Food and Drug Administration's user fee and seven years market exclusivity on drugs that have no economic viability.

 

The first vouchers can be legally issued from 27 September 2008. But the wording of the voucher law needs tightening up, say commentators, and some aspects — such as a rule stating that drugs can't contain active ingredients that have been approved in another application — could restrict eligibility. The Food and Drug Administration is currently drawing up guidelines on how the law will work in practice.

 

Masters exclusively distributes Benznizadole for the treatment of Chagas Disease, a tropical disease largely prevelant in Latin America. For more information, please contact Robert Smith at Masters Brazil ( This email address is being protected from spam bots, you need Javascript enabled to view it ).

 
MHRA approves first OTC Chlamydia treatment

The Medicines and Healthcare products Regulatory Agency (MHRA) has approved the first over the counter  medicine to treat chlamydia. The azithromycin pill, sold under the brand name “Clamelle”, will be available to buy by people aged 16 and over, if they have tested positive for the infection and have no symptoms, and for their sexual partners.

 

For more information, please refer to the MHRA website .

 
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