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Drugs and Cosmetics act, 1940

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regarding DTAB, DCC and CDL constitution and function

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Drugs and Cosmetics act, 1940

  1. 1. Drugs and Cosmetics Act, 1940 and Rules, 1945 “DTAB, DCC and CDL- Constitution and Function” Presented to: Presented by: Ms. Nitu Singh Payal R. Mundada Dept. of Pharmacognosy Pharm. D. III year
  2. 2. “Administration of the Act & Rules” • Drugs Technical Advisory Board • Drugs Consultative Committee • Central Drugs Laboratory • Drugs Control Laboratories in state • Government Analysts • Licensing Authorities • Controlling Authorities • Drug Inspectors • Customs Collectors
  3. 3. “DTAB”- Drugs Technical Advisory Board Constitution :  This Board was constituted by the Central Government.  This Board shall consist of the following 18 members: 5 elected 5 nominated 8 Ex- officio
  4. 4. Ex-officio : • Director General of Health Services (Chairman) • Drugs Controller of India • Director, CDL, Kolkata • Director, CRI, Kasauli • Director, IVRI, Izatnagar • President, PCI • President, MCI • Director, CDRI, Lucknow Nominated : • 2 persons- nominated by Central Govt. amongst persons incharge of drugs control in States • 1 person- nominated by Central Govt. from pharm. Industry • 2 Govt. Analysts- nominated by Central Govt. Elected : • A teacher- pharmacy or pharm. chem. or cognosy on staff of an Indian Uni or an affliated college- elected by Executive committee of PCI • A teacher- medicine or therapeutics…….. MCI • 1 pharmacologist- by Governing body- ICMR • 1 person- by Council of CMA • 1 person- Council of IPA
  5. 5. Functions :  This Board was constituted with a purpose to advise the Central and State Govts. on technical matters arising out of the administration of Drugs and Cosmetics Act, 1940.  Nominated and elected members hold the office for- 3 years and are eligible for re- nomination or re- election.  Central Govt. appoints a Secretary and provides clerical staff.  The Board, with previous sanction of C. Govt., make by- laws fixing quorum and regulating its own procedure and the conduct of the business to be transacted by it.  The Board may constitute sub-committees and appoint temporary members for =< 3 years.
  6. 6. “DCC”- The Drugs Consultative Committee Constitution :  This advisory committee was constituted by the Central Government.  The committee shall consist of the following members: Representatives of the Central Government 2 Representative of each State Government 1
  7. 7. Functions :  This committee was formed in order to secure uniformity in the D&C, Act 1940 throughout India.  It advises the Central Govt., State Govt., and even DTAB on matters tending to secure uniformity.  The DCC meets when required by Central Govt.  Empowered to regulate its own procedure.
  8. 8. “CDL”- The Central Drugs Laboratory Established in Kolkata, CDL is the national statutory laboratory of the Government of India. It is under the control of a Director appointed by the Central Government.  It is the oldest quality control laboratory of the Drug Control Authorities in India.
  9. 9. Procedure : Samples sent by the court for analysis to the CDL by a registered post in a sealed packet Enclosed with a memorandum in prescribed form , in an outer cover addressed to the Director Packet and outer cover marked with a distinguished number A copy of memorandum and specimen impression of seal sent separately by registered post to the Director On receipt of the packet, it should be opened by an authorized person on behalf of the Director The condition of the seal on the packet to be recorded Result of test to be sent to the sender Certificate issued by CDL should be signed by the Director or any officer authorized by the Central Govt. on his behalf
  10. 10. Functions :  To analyze drugs and cosmetics samples sent by Customs Collector or Courts.  Analytical Quality Control of the imported samples.  Any other duties entrusted by the Central Government.  Preparations of reference standards and their maintenance.  Maintenance of microbial cultures.  Acting as an appellate authority in matter of disputes.
  11. 11. “References”  www.cdsco.nic.in  “Pharmaceutical Jurisprudence”, Jani GK, Atul Prakashan, Fifth Edition- 2005-06; 28.  “A textbook of Forensic Pharmacy”, Jain NK, Vallabh Prakashan, Eighth thoroughly revised edition; 147-149.  "India's Central Drugs Standard Control Organization (CDSCO)". Pacific Bridge Medical. Dec 29, 2012. Retrieved Dec 29, 2012.

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