Kokate Committee
Constitution: The Kokate Committee was constituted by Ministry Of Health And Family Welfare, Government of India, under the chairmanship of Prok. C.K. Kokate, VC, KLE University, Belgaum, Karnataka.(1) The need to constitute the Kokate Committee: Drug Controller General India (DCGI) had issued a letter dated 15.01.2013 to all the State […]
Draft Guidelines on Similar Biologics, 2016
Medicinal products which are mainly composed of living tissues or cells are called Biologics
Read MoreMEDICAL DEVICE REGISTRATION IN INDIA
Medical device industry is still nascent in India, most devices are manufactured globally and imported
Read MoreFSSAI Draft Norms for E-Commerce FBO’s
To ensure safety FSSAI has come up with draft norms for e-commerce FBO's. It is now mandatory to obtain licenses for all online Food Businesses and supply chain
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New Medical Device Rules To Be Rolled Out In 2018
The Drugs and Cosmetics Act, 1940, has been governing drugs and medical devices since 1940 and has received multiple iterations each year. Owing to the significant changes that have occurred in the healthcare and pharmaceutical industry and constant requests from leaders in these industries, an overhaul was long overdue. In […]
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Sugam Portal – CDSCO Sugam Registration for Online Application
Indian Government has chosen to join the foray and ride the digital wave through SUGAM, launched on 14 November, 2015
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FSSAI Regulations for Caffeinated Beverages
FSSAI has added standards for caffeinated beverages and use of blue tint in the plastic bottles related to beverages non-alcoholic carbonated food products
Insight
Medical Devices Rules 2017: An Overview
CDSCO issued a draft of Medical Devices Rules, 2016 through a gazette notification (No. 724) published on October 17, 2016
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India Champions e-Governance for Pharma Industry
National e-Governance plan (NeGP), launched in 2006 as initiative that Government of India has implemented to make all government services accessible online.