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Drive For Good Quality Medicines, Foods Reinforced By USP Agreements With Chinese Drug Authorities
As part of its efforts to improve the quality of medicines and food ingredients worldwide, the U.S. Pharmacopeial (USP) Convention this week reached three new cooperative agreements with Chinese drug control authorities. Because Chinese manufacturers supply so much of the world"s drug and food ingredients, these agreements-coupled with three previous agreements between USP and other government organizations in China-mark a significant commitment to ensure that concerns about quality are addressed. USP is a scientific, nonprofit organization that sets standards for the quality of prescription and over-the-counter drugs that are enforced by the U.S. Food and Drug Administration (FDA) in the United States. USP also sets standards for the quality of food ingredients and dietary supplements; these and USP"s drug standards are used in more than 130 countries.
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China Aoxing Pharmaceutical Company Acquires A Novel Menstrual Pain Drug
China Aoxing Pharmaceutical Company, Inc. (OTCBB: CAXG) ("China Aoxing"), a pharmaceutical company specializing in research, development, manufacturing and marketing of narcotic and pain-management products, announced that it has acquired all rights to TJSL, a novel drug at Phase II development stage to treat primary dysmenorrhea ("PD"), or menstrual pain, in adult women.
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Massachusetts Proposal To End Fee-For-Service Could Be National Model
A proposal in Massachusetts to end the practice of paying doctors for individual procedures could prove a model to hold down costs for U.S. health care reform, Reuters reports.
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Society Welcomes Decision On Ephedrine And Pseudoephedrine

The Royal Pharmaceutical Society welcomed the decision by the Medicines and Healthcare Products Regulatory Agency that medicines containing ephedrine and pseudoephedrine should retain their status as pharmacy (P) medicines. President Steve Churton said: "We are delighted at the MHRA"s decision to keep cold and flu remedies containing ephedrine and pseudoephedrine as pharmacy (P) medicines. "The decision is a ringing endorsement of the vigilance pharmacists have shown in monitoring and controlling the sale of these products. "Pharmacists are experts in medicines and experienced in dealing with medicines liable to misuse. The MHRA"s decision is great news for consumers and provides a clear signal of faith in the pharmacy profession. "I urge pharmacists to continue to remain alert to the supply of these medicines so that they continue to keep their P status". Notes The MHRA have taken this decision taken following the review by the Commission on Human Medicines (CHM) of the measures introduced from July 2007 to control the risk of misuse of OTC medicines containing pseudoephedrine and ephedrine, in the manufacture of the Class A controlled drug methylamphetamine http://www.mhra.gov.uk Royal Pharmaceutical Society


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