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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Oct
9
2017
FDA Draft Guidance Addresses Medical Device Status of Microneedling Products Covington & Burling LLP
Sep
30
2018
The Week Ahead in the European Parliament – September 28, 2018 Covington & Burling LLP
Oct
5
2018
UK Government Issues “No Deal” Brexit Notices for the Food & Beverage Sector Covington & Burling LLP
Oct
22
2018
The European Commission finds no illegal State aid was provided by Luxembourg’s non-taxation of McDonald’s Covington & Burling LLP
Nov
8
2018
Drug Pricing In The New Congress Covington & Burling LLP
May
19
2014
China Restructures Its Medical Device Regulatory System Covington & Burling LLP
Jun
4
2014
China Food & Drug Administration Releases Draft Measures On Unannounced Pharmaceutical Drug Inspections Covington & Burling LLP
Jul
28
2014
FDA Finalizes Guidance on the Evaluation of 510(k) Substantial Equivalence Covington & Burling LLP
Aug
4
2014
Commission Updates EU Medical Devices Borderline Manual Covington & Burling LLP
Sep
22
2014
White House Mobilizes Forces Against Superbug Covington & Burling LLP
Oct
8
2014
EU Consultation on the Development of Criteria to Identify Endocrine Disruptors in Biocidal and Plant Protection Products Covington & Burling LLP
Jan
14
2015
Latest Proposal to Repeal Medical Device Excise Tax Gains Traction Covington & Burling LLP
Mar
3
2015
Details Of The European Commission’s Legal Analysis Of ‘Reverse Patent Settlement Agreements’ Revealed Covington & Burling LLP
Apr
7
2015
CMS Releases New Reimbursement Guidance for Biosimilars Covington & Burling LLP
Jun
12
2015
General Court Confirms Market Exclusivity Rights in CTRS Case Covington & Burling LLP
Jan
8
2016
New EU Novel Foods Regulation: Step Towards Simpler and Faster Procedure? Covington & Burling LLP
Apr
3
2017
The Week Ahead in the European Parliament – March 31, 2017 Covington & Burling LLP
May
5
2017
EU Policy Update, May 2017: Brexit and European Elections; Tech and Digital Single Market; Communication and Media; Energy and Environment; Internal Market and Financial Services; Life Sciences and Healthcare; Trade Policy and Sanctions Covington & Burling LLP
Jun
29
2017
EU Vote on First Borderline Decision Confirms: Cranberry Products Are Not Medical Devices Covington & Burling LLP
Oct
18
2017
FDA Finalizes Guidance on Medical Product Classification Covington & Burling LLP
Jun
24
2014
Food and Drug Administration (FDA) Relaxes Regulation of Certain Software Devices Covington & Burling LLP
Sep
11
2014
Court of Federal Claims Stays Decision Requiring Commercial Item Contractor to Comply with Non-Commercial Practices Covington & Burling LLP
Nov
5
2014
Custom Device Exemption Remains Narrow, but FDA’s Final Guidance Addresses Industry Concern About “Device Type” Definition Covington & Burling LLP
Jan
21
2015
New French Rules On Off-Label Use Covington & Burling LLP
Oct
11
2016
Dynamic Political and Public Policy Landscape in DC on Pharmaceutical Issues Covington & Burling LLP
Dec
23
2017
FDA Publishes Draft Guidance on Investigational IVDs Used in Therapeutic Product Clinical Trials Covington & Burling LLP
Jul
30
2014
European Commission Fines Servier and Five Generic Companies for Preventing Entry of Generic Versions of Blood Pressure Control Drug Covington & Burling LLP
Aug
5
2014
The Electronic Wallet System: How Nigeria Is Dialing Into Its Agricultural Sector Covington & Burling LLP
Aug
29
2014
Pharmacies Avoid False Claims Act Suit: Fox Rx Inc. v. Omnicare Inc. et al. Covington & Burling LLP
Jan
4
2015
Changes to Biofuels Provisions in House-Passed NDAA FY 15 Covington & Burling LLP
Apr
8
2015
European Union Policy Update—April re: Digital Single Market Policy, Finance, Life Sciences and More Covington & Burling LLP
Aug
6
2015
Bill Introduced to Streamline and Clarify Combination Product Regulatory Process Covington & Burling LLP
Oct
27
2015
Recent Reports Claim Improvements in FDA’s Review of Medical Device Submissions Covington & Burling LLP
Mar
16
2018
The Long-Standing TAA “Substantial Transformation” Standard for Drug Products is Challenged at the Court of International Trade Covington & Burling LLP
Apr
13
2018
The Week Ahead in the European Parliament – April 13, 2018 Covington & Burling LLP
 

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