Mondaq India: Food, Drugs, Healthcare, Life Sciences
S.S. Rana & Co. Advocates
Food Safety and Standards Authority of India (hereinafter referred to as "FSSAI") is responsible for regulating genetically modified (hereinafter referred to as "GM") food products.
Singh & Associates
Drug Repurposing, the emerging trend resulting from increasing cost of new drug discovery, researches, trails and generic competition.
Khaitan & Co
The purpose of the Legal Metrology (Packaged Commodities) Rules, 2011 (PCR) is to regulate pre-packaged commodities. Under the PCR, pre-packaged commodities must comply with certain mandatory labelling requirements.
Vaish Associates Advocates
The ‘medical devices' sector has largely enjoyed a free hand from the regulators in India, as the sphere has largely gone unregulated thus far.
Singh & Associates
The Uniform Code of Pharmaceuticals Marketing Practices, 2014 ("UCPMP Code") is a voluntary code issued by the Department Of Pharmaceuticals ("the Department") relating to marketing...
LexOrbis
Rich and varied biodiversity, accompanied by an extensive traditional and contemporary knowledge system makes India one of the most diverse nations in the world in this regard.
Khaitan & Co
Access to affordable and safe medicines is the cornerstone of a vibrant public health framework.
Duane Morris LLP
New Purchased/Referral Care (PRC) regulations give the Indian Health Service (I) , Tribal Organizations (T) and Urban Indian Organizations (U) the ability to cap payment rates...
SKP Business Consulting LLP
Since the government declared medical devices as one of the 25 focus sectors in 2014, the industry has been undergoing significant changes in terms of new policy measures and strengthening of the regulatory framework.
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.
Most Popular Recent Articles
Khaitan & Co
The purpose of the Legal Metrology (Packaged Commodities) Rules, 2011 (PCR) is to regulate pre-packaged commodities. Under the PCR, pre-packaged commodities must comply with certain mandatory labelling requirements.
Vaish Associates Advocates
The ‘medical devices' sector has largely enjoyed a free hand from the regulators in India, as the sphere has largely gone unregulated thus far.
Infini Juridique
Government of India has announced the START UP India in August 2015. Under "START UP INDIA", the Govt. intends to build a strong eco system for nurturing innovation and start ups in the country ...
Singh & Associates
In the words of advertising tycoon Leo Burnett, "Let's gear our advertising to sell goods but let's recognize also that advertising has a broad social responsibility."
Tuli & Co
Health insurance business in India has, traditionally, been regulated by the framework governing general insurance business as issued by the Insurance Regulatory and Development Authority of India (IRDAI)...
SKP Business Consulting LLP
Since the government declared medical devices as one of the 25 focus sectors in 2014, the industry has been undergoing significant changes in terms of new policy measures and strengthening of the regulatory framework.
Khaitan & Co
At present, the Drugs and Cosmetics Rules, 1945 (Drugs Rules) regulate 15 categories of medical devices as drugs.
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
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.
LexOrbis
The Indian pharmaceutical industry is a major manufacturer of cost-effective generic drugs and is set to become the leading exporter of generic pharmaceutical products.
Article Search Using Filters
Related Topics
Popular Authors
Popular Contributors
Up-coming Events Search
Tools
Font Size:
Translation
Channels
Mondaq on Twitter
Partners
In association with