'Cosmetics act' presentation slideshows

659 views • 47 slides

Infrastructure & Regulatory Aspect of Ayurvedic, Siddha & Unani Indian Traditional Medicines in India

Infrastructure & Regulatory Aspect of Ayurvedic, Siddha & Unani Indian Traditional Medicines in India. . TRADITIONAL HEALTH KNOWLEDGE SYSTEM OF INDIA * Rich biodiversity,one of the Richest medicinal plants flora

1.92k views • 40 slides

HEALTH HERITAGE

HEALTH HERITAGE. SANGAM* OF ANCIENT WISDOM AND MODERN SCIENCE R.R. Hirwani Head CSIR Unit for Research and Development of Information Products, Pune, India GRA MEETING 1 February 2006. *SANGAM ~ CONFLUENCE.

707 views • 37 slides

Soils, Agriculture, Fisheris Jeopardy!

373 views • 37 slides

Dr. A. Ramkishan M.Pharm , PhD. FIPS, FTASc , FIPA. Deputy Drugs Controller (India)

Regulatory Tools ensuring transparency of Registration and Inspection Procedures for entering into the Indian Market. Dr. A. Ramkishan M.Pharm , PhD. FIPS, FTASc , FIPA. Deputy Drugs Controller (India) Central Drugs Standard Control Organization (CDSCO),

406 views • 15 slides

International Medical Products Anti-Counterfeiting Taskforce

387 views • 12 slides

Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)

354 views • 12 slides

Regulating Food Additives

285 views • 6 slides

Operon strategist Provide guideline For CDSCO Registration and Wholesale License Certificates of Medical Device Contact details u2013 Phone no - 9325283428 Mail - dm@operonstrategist.com Visit u2013 https://www.operonstrategist.com/cdsco-license-wholesale-registration/?utm_source=classified submission&utm_medium=classified page&utm_campaign=classified submission

74 views • 6 slides

The Federal Food, Drug, and Cosmetics Act

The Federal Food, Drug, and Cosmetics Act. Ashley Nunez 1A. The FDCA is a set of laws passed by congress in 1938 It was amended about 7 times between 1906-1935 It is a national law of the United States. This act was introduced by the death of more than 100 patients.

223 views • 4 slides

GOI Classifies Some Medical Devices as Drugs

The Ministry of Health and Family Welfare, GOI recently released a draft notification concerning the classification of certain medical devices as drugs. The draft was released in October, 2019 and suggestions were invited from the public and stakeholders for finalizing it as a new addition to the Medical Device Rules, 2017.

31 views • 3 slides