Mondaq All Regions - India: Food, Drugs, Healthcare, Life Sciences
Singh & Associates
The calculation methodology of the fixation of price for drugs is a complicated one and recently we have come across yet another case of using incorrect methodology for price fixation...
S.S. Rana & Co. Advocates
In 2015, India's apex food regulator, theFSSAI, had ordered recall of energy drinks, Tzinga, Cloud 9, Monster Energy from the market declaring ingredients in these energy beverages were not safe.
Nishith Desai Associates
The Central Government has clarified that the institutional collaboration between Bill & Melinda Gates Foundation and National Technical Advisory Group on Immunization is not financially linked.
S.S. Rana & Co. Advocates
The Government of India, under the aegis of Ministry of Health and Family Welfare has notified the Medical Devices Rules, 2017, which is scheduled to come into force on January 1, 2018.
Khaitan & Co
At present, the Drugs and Cosmetics Rules, 1945 (Drugs Rules) regulate 15 categories of medical devices as drugs.
Nishith Desai Associates
United States pharmaceutical giant Merck & Co., Inc. (known as Merck Sharp & Dohme (MSD) outside the United States and Canada), through its subsidiaries, divested its 6 brands to Zydus Cadila's wholly owned subsidiary Zydus Healthcare Limited.
Nishith Desai Associates
The medical device industry is, without a doubt, one of India's sunrise industries as it has consistently outshone many other industries in terms of year on year growth.
ARA LAW
While the economy is witnessing a fast transition from "offline" to "online" markets and there is a sturdy buzz of "demonetization" and "one click" access to everything, . . .
Khaitan & Co
FDCs are combinations of two or more active pharmaceutical ingredients in fixed ratios, given in the form of a single dose.
Kochhar & Co.
Food processing includes all the processes under filtration, manufacturing and preservation techniques undertaken for bringing value addition to the agricultural or horticultural produce.
S.S. Rana & Co. Advocates
CDSCO is the national regulatory authority in India that evaluates safety, efficacy and quality of drugs in the country.
Khaitan & Co
The Hon'ble Supreme Court of India has, in the case of State of Uttar Pradesh v Dr Dinesh Singh Chauhan, struck down the practice of grant of reservation for in-service candidates in post graduate medical degree courses.
Singh & Associates
The regulatory framework relating to clinical trial of drugs is governed under the Drugs and Cosmetics Act, 1940 ("Act") and the Drugs and Cosmetics Rules, 1945.
Singh & Associates
In an information release by Press Information Bureau on 14th May 2016, Ministry of AYUSH Government of India and the World Health organization (WHO) have signed an historic Project Collaboration Agreement (PCA) for cooperation on promoting the quality, safety and effectiveness of service provision in traditional and complementary medicine.
Nishith Desai Associates
TPG Growth has acquired a significant majority stake in Bengaluru based Rhea Healthcare Pvt. Ltd. as its recent investment in healthcare space in India.
Deloitte
In 2014 we published a report on End of Life Care in the UK and subsequently have written a number of related blogs on this important subject.
TMT Law Practice
""If I said tennis is totally clean, I would be kidding myself [..] I would say there are certainly some short cuts being taken. Not that many, but it would be crazy to think differently." - Nick Bollettieri
PSA Legal Counsellors
This move not only makes clinical trials for academic research on drugs more cost effective and efficient, but also promotes innovation in terms of treatment of critical maladies like AIDS, cancer, etc.
Khaitan & Co
The Competition Appellate Tribunal (COMPAT) on 10 May 2016 has passed a landmark decision setting aside the Competition Commission of India's (CCI) decision in P K Krishnan v Paul Madavana and Ors.
Nishith Desai Associates
A Roundtable on Cloud Computing – Privacy, Security & Legal Compliance Considerations in the Digital Transformation of Healthcare in India, Part 3 (Apr 26, 2016).
Most Popular Recent Articles
Khaitan & Co
The Hon'ble Supreme Court of India has, in the case of State of Uttar Pradesh v Dr Dinesh Singh Chauhan, struck down the practice of grant of reservation for in-service candidates in post graduate medical degree courses.
Singh & Associates
The report highlighted for the need for a central legislation for registration of clinical establishments in the country and uniform standards need to be developed for the entire country.
Singhania & Partners LLP, Solicitors and Advocates
The Food Safety and Standards Authority of India (FSSAI), India's food regulator has issued new norms for the import, labelling and packaging of products imported to India...
Khaitan & Co
At present, the Drugs and Cosmetics Rules, 1945 (Drugs Rules) regulate 15 categories of medical devices as drugs.
Singh & Associates
The Core-Committee (Committee) constituted by the Ministry of Health & Family Welfare (MOHFW), Government of India, reviewed and revised the National List of Essential Medicines...
Singh & Associates
The recent controversy with respect to MNC Giant Nestle's Maggie noodles across the country has once again opened the Pandora box with respect to dual safety standards being followed by the MNC food company in the Country.
Nishith Desai Associates
The Central Government has clarified that the institutional collaboration between Bill & Melinda Gates Foundation and National Technical Advisory Group on Immunization is not financially linked.
S.S. Rana & Co. Advocates
The Government of India, under the aegis of Ministry of Health and Family Welfare has notified the Medical Devices Rules, 2017, which is scheduled to come into force on January 1, 2018.
Nishith Desai Associates
United States pharmaceutical giant Merck & Co., Inc. (known as Merck Sharp & Dohme (MSD) outside the United States and Canada), through its subsidiaries, divested its 6 brands to Zydus Cadila's wholly owned subsidiary Zydus Healthcare Limited.
Nishith Desai Associates
The medical device industry is, without a doubt, one of India's sunrise industries as it has consistently outshone many other industries in terms of year on year growth.
LexCounsel Law Offices
The Central Drugs Standard Control Organization ("CDSCO") has released draft guidelines in an effort to streamline the regulatory process for granting marketing permission to similar vaccines and other biosimilars in India.
Singh & Associates
Post marketing surveillance is performed after market approval/clinical trials of drugs in India.
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