pratiyogita darpan hindi Published this article page no 119 Draft also proposes regulation of devices will be under a separate Act and not under Drugs and Cosmetics Act 1940 as was being pushed by Health Ministry. Central Drugs Standard Control Organisation (CDSCO) CDSCO under Directorate General of Health Services Ministry of Health & Family Welfare is the National Regulatory Authority of India. Its headquarter is located at New Delhi. Under the Drugs and Cosmetics Act CDSCO is responsible for approval of Drugs Conduct of Clinical Trials laying down the standards for Drugs control over the quality of imported Drugs and coordination of the activities of State Drug Control Organizations. CDSCO along with state regulators is jointly responsible for grant of licenses of certain specialized categories of critical Drugs such as blood and blood products I. V. Fluids Vaccine and Sera. E.g. a small manufacturer of masks or neck bracing collars would find it difficult to hire a qualified QMS manager with biomedical engineering. Against the expectations of the domestic medical device industry to have a separate law (to regulate medical devices) the government has come up with the current rule that defines such devices as drugs and brings it under the purview of Drugs and Cosmetics Act for regulatory approval. o Any nonconformity under Drugs and Cosmetics Act can be treated as a criminal offence by a drug inspector at his discretion and taken before a court without any risk proportionate penalties pratiyogita darpan hindi buy.
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