Biotech, Food, Drug

The food we eat and the medicine we put into our bodies are highly regulated by a variety of government agencies. In the United States by the Food and Drug Administration (FDA) and the United States Department of Agriculture (USDA) regulate the processes by which food makes its way to the grocery store and medicine is approved for consumer use.  As the science grows more complex behind the pharmaceutical and food industry, interpretation of the regulations in place is becoming more nuanced.  Overseas, these industries are regulated by a variety of agencies; for example, the Minister of Agriculture in Canada, Centre for Food Safety in Hong Kong, and the Committee of Environmental, Public Health and Food Safety (EU), are among the many governing-bodies which regulate biotechnology, food, and drugs throughout the world.

The National Law Review is your free online resource to agency news, emerging topics in food and drug, and the latest in biotechnology updates. From nanotechnologies being used in research, to regulations of imported foods coming into the US from overseas or the development of medical devices and drugs, readers can find expert legal analysis of the developments in the industry, as well as reports on changes within the agencies that regulate these industries. The National Law Review also covers topics related to licensing, Food Safety and Inspection Services (FSIS), food and beverage regulation in the US and worldwide, nutrition labeling, and country of origin labeling guidelines.

With recent legislation being passed throughout the US in relation to marijuana use, both for recreational and medicinal purposes, readers will also find up-to-date information, litigation, and news coming from this area of interest as well. Regulations in California for labeling and proper sales of marijuana, to use in different states, or internationally, as well as rules for promoting and advertising marijuana are also covered on the site. Additionally, the development and changing landscape of tobacco use to include vaping, and how e-cigarettes and vaping are regulated, is also covered by NLR authors.

Readers who are interested in food safety, inspection, imports into the US, and regulations, these topics are covered regularly on The National Law Review as well. New legislation from the FDA, USDA, Department of Agriculture, and international bodies, are covered on the site. If you are looking for details on new nutrition-labeling regulations or health risks of consuming certain imported foods, you will find these topics, and many more, on The National Law Review.

For hourly updates on the latest news about biotech, food & drug, and cannabis laws, regulations, and legislation, be sure to follow our Cannabis Twitter feed, and sign up for complimentary e-news bulletins.

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Sep
5
2017
The UK’s Life Sciences Industrial Strategy: Digital Health Implications Covington & Burling LLP
Sep
13
2014
Judge Requires PhRMA To Initiate New 340B Orphan Drug Lawsuit to Challenge Interpretive Rule Covington & Burling LLP
Sep
25
2014
Recent Settlement Highlights Importance of Tracing Country of Origin When Selling Medical Devices to the U.S. Government Covington & Burling LLP
Oct
11
2014
Pharmaceutical Research and Manufacturers of America (PhRMA) Filed Suit Today Seeking to Invalidate the 340B Orphan Drug Exclusion Interpretative Rule Covington & Burling LLP
Feb
2
2015
EMA Transparency Policy – EMA Launches Public Consultation On The Publication Of Information Under The New EU Clinical Trials Regulation Covington & Burling LLP
Apr
20
2015
China FDA Focuses on Enforcement of Medical Device Good Manufacturing Practices Covington & Burling LLP
Sep
16
2015
CDRH Schedules Next Generation Sequencing Workshops Covington & Burling LLP
Jul
20
2016
Italian Administrative Court Finds That All Non-Prescription Medicines May Be Advertised to the Public Covington & Burling LLP
Dec
9
2016
The Week Ahead in the European Parliament – December 9, 2016 Covington & Burling LLP
Dec
23
2016
Twenty-First Century Cures Act Includes HIPAA Provisions Covington & Burling LLP
Apr
10
2017
The Week Ahead in the European Parliament – April 7, 2017 Covington & Burling LLP
Jul
14
2017
EU Policy Update, July 2017: Brexit and Elections in the UK and France; Tech and Digital Single Market Policies; Communication and Media Policies; Energy and Environment Policies; Internal Market and Financial Services Policies Covington & Burling LLP
Sep
22
2017
AG’s Opinion – Licensed and Unlicensed Medicines May Fall Within the Same Relevant Product Market Covington & Burling LLP
Dec
15
2017
Digital Health Checkup (Bonus): Product Liability and Insurance Coverage Covington & Burling LLP
Jan
10
2018
Insurance Coverage for Opioid Lawsuits & Investigations Covington & Burling LLP
May
23
2014
Senate Republicans Press Food and Drug Association on Draft Guidances Covington & Burling LLP
Jun
7
2014
FDA Issues Draft Guidance on Voluntary Consensus Standards Covington & Burling LLP
Jul
23
2014
New Food Safety Law for China Covington & Burling LLP
Jul
31
2014
FDA Finalizes Appeals Guidance on Section 517A of the Food, Drug, and Cosmetic Act Covington & Burling LLP
Nov
21
2014
The German Supreme Administrative Court Confirms That E-Cigarettes Are Not Medicines Or Medical Devices Covington & Burling LLP
Dec
13
2014
Comprehensive New EU Food Labeling Regulation Goes Into Effect December 13 Covington & Burling LLP
Dec
18
2014
Indonesia — Can it Unleash Needed Investment? Covington & Burling LLP
Jan
20
2015
CFDA Proposes New Regulations on the Accreditation of Medical Device Trial Sites: China Food and Drug Administration Covington & Burling LLP
Feb
9
2015
FDA Issues Draft Guidance on Combination Product Manufacturing Covington & Burling LLP
Mar
31
2015
German Exemptions from Mandatory Rebates for Pharma Companies Are in Line with EU State Aid Rules Covington & Burling LLP
Aug
20
2015
Italian Medicines Agency Makes Public Assessment Reports Available on its Website Covington & Burling LLP
Jul
15
2016
B2B or not B2B: Application of the NHCR to Business-to-Business Commercial Communications Covington & Burling LLP
Oct
7
2016
EU Policy Update, October 2016: Brexit and the EU’s Response; Communication and Media Policies; Energy and Climate Change Policies; Trade Policy and Sanctions Covington & Burling LLP
Dec
12
2016
China Food and Drug Administration Releases Draft Classification Catalogue of Medical Devices Covington & Burling LLP
Jan
18
2017
FDA Issues Discussion Paper on Possible Regulatory Approach for Laboratory Developed Tests Covington & Burling LLP
Feb
8
2018
Hoffmann-La Roche – Some Broader Implications Covington & Burling LLP
Apr
29
2014
Innovations in Vaccine Delivery in Africa Covington & Burling LLP
Sep
16
2014
President Obama’s Response to the Ebola Crisis Covington & Burling LLP
Oct
13
2014
Contract Farming in Africa Increases Productivity, Reduces Post-Harvest Loss Covington & Burling LLP
Jan
8
2015
FDA Issues Draft Guidance on 510(k) Transfers Covington & Burling LLP
 

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