Guest guest Posted January 24, 2008 Report Share Posted January 24, 2008 Dear Dr.V.Thawani! Before i proceed to get-back-gesture in netrum- i should first fill this interesting feature....!! i had already copied this whole reference just after seeing your mail, on Hath......, then i opened up,to post here at netrum... Sir i got some more findig/report as below--sply in last two paragraphs: There is no national list of essential drugs although some recommendations have been made. There is no mechanism for monitoring and documenting adverse drug reactions. There is no approval process for drugs within the market having drugs with no proven benefit, some with opium content, some with combinations of steroids are on the market. There are 4 ineffective Central Drugs Standard Control Organizations in Bombay, madras, Calcutta, and Cochin.The State Trading Corporation (STC) has the responsibility for importing raw materials and distributing them to private and public manufacturers. The Indian Drugs and Pharmaceuticals, Ltd. within the Ministry of Industry is responsible for drug pricing and controlling raw materials for the manufacture of drugs within the country. Quality control of all medications within the country is the responsibility of the Ministry of Health and Family Welfare. There is a drug formulary with a limited circulation. In 2000, there were new regulations to control the quality and standard manufacturing practices of Indian herbal medications. There are 9,000 traditional medications that the government wants to certify with good manufacturing principals. The existing laboratories were upgraded and ten new laboratories were established for testing of traditional medications. Randomized clinical trials have been established. In 1972, 39 percent of the of drug production was by 50 privately owned Indian drug firms, 34 percent by two large government firms, and 27 percent by foreign owned firms located in India. In 2000, the top 20 firms in the nation controlled 70 percent of the market. There were 9,000 small firms in the nation with an increase to more than 20,000 firms in 2000. There are 63 foreign companies producing medications in the nation. Unfortunately most of the drug companies produce very few bulk drugs needed for the masses. Most of the companies produce formulations or finished products that are 89.38 percent of all the goods produced. The multinationals also sell medications in India that are not for sale in their native country, but which have significant side effects. In 1994, there were more than 50,000 brand name products in the nation. In 2000, there were several firms that were selling " copy cat " medications. This was a major threat to the established manufacturing producers and importers. Cipla sold its medications for 2 to 5 percent of the price of the equivalent medication in the United States. The biggest rival to Cipla is Ranbaxy. Other significant firms are Dr. Reddy's, Wockhardt, and Sun Pharma. This practice is legal under Indian Law. Patents cover the process of manufacturing and not the products themselves. Many medications are produced by reverse engineering. These firms have none of the overhead that is associated with new medications trials and approval. Unfortunately not all the firms produce quality products and there have been cases of weak or toxic medications. Fortunately for the world market, in 1994 India became a signatory of the treaty on intellectual property of the World Trade Organization. This treaty required India to recognize patents by the year 2005. Para1 Meanwhile, in 1975, the Hathi Commission presented a report dealing with the shortfalls and supply of medications in the nation. Foreign nations were asked to limit their foreign equity share to 40 percent or less. An attempt to correct the shortfall of bulk drugs for the masses was by the state owned pharmaceutical companies (Bengal Chemical and Pharmaceutical Limited, Bengal Immunity Limited, Hindustan Antibiotic Limited, Indian Drugs and Pharmaceuticals Limited, and Stanistreet Pharmaceutical Limited). They were to manufacture and supply the 117 designated basic needed drugs that are affordable to the masses. All new registered drugs were to be designated by the generic names. Generic designations were to be displayed more prominently than the brand names. Unfortunately, the government companies suffer with obsolete plan and equipment, decreased capital, decreased technology, and the competitive pressure from the commercial sector. The state companies have difficulty in supplying ten percent of the needs. In 1980, essential drugs were only 28 percent of the total produced. Luxury medications and those for wealthier clientele are oversupplied with 1,000 vitamins, 700 tonics, and 400 sedatives on the market. Para2 The prescribing of medications by physicians purportedly enhances their position. The population feels the need to consume medications to effect a cure. There is an over prescribing of medications, especially antibiotics. In 1975, the Hathi Committee proposed a list of 117 essential drugs. Other findings of the Hathi Committee by the pharmaceutical companies and the business community approved the many non-essential drugs on the market, with 16 percent of the purchases tonics and multivitamins. There are 80,000 formulations of medications sold in the country. In 1980, India had 1.9 percent of the world's total drug consumption with 80 percent from a commercial source. Medications at the primary care clinics are in short supply and usually received after care is needed. 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