Biotech, Food & Drug

HB Ad Slot
HB Mobile Ad Slot

In today’s hyper-aware environment, concerns about food and drug safety are paramount for both companies and consumers.  The Food and Drug Administration (FDA) and the US Department of Agriculture (USDA) regulates the areas of biotech, food, and drug law. Additionally, laws including the 21st Century Cures Act, and cGMP (Current Good Manufacturing Processes), regulate industry standards/norms in food, cosmetics, and other industry-sectors. Visitors to the National Law Review will find the latest analysis of news, legislation, and upcoming cases/litigation as it relates to this area of law.

With researchers searching for new energy solutions and other developments in biotech, visitors to the NLR will have the opportunity to read content surrounding biosimilars, natural fuel production, medical devices, biotechnology, nanotechnology and materials, and the pharmaceuticals industry. Additionally, content relating to food and drug laws, limits on chemical use in cosmetic products, and other general health/safety topics are covered by the National Law Review and are updated regularly. Additionally, food safety and imports to the United States are also discussed as they become relevant. 

In addition to general health, science, and food/drug, the industry is also closely related to many of the issues related to intellectual property law. New applications for patents, intellectual property, licensing laws, and other areas which are governed by the PTAB court, often crossover into the industry.

New developments in legislation, including the legalization of recreational marijuana has created a new area ripe for legal analysis.  Regulations on how recreational marijuana can be advertised and marketed, distributed and the kind of insurance coverage necessary for dispensaries.  Additionally, employer drug-testing and marijuana statutes have been a hot area of litigation covered by the National Law Review.  

General practices in marketing standards, compliance of federal and state laws/legislation, licensing collaborations, and news related to bringing new products to the market, in the US and abroad, are among the areas visitors to NLR will read about daily. Drug pricing, changes in production standards, regulatory compliance, food safety and handling, drug laws (legalization of marijuana, both recreational and medicinal in the workplace), and labeling and nutritional requirements, are among the many topics covered by the National Law Review daily.

Visitors will always find the latest, up-to-date, most comprehensive coverage on the site. And, news and stories which affect the US, companies which are regulated in the industry, and multinational/international companies, are detailed regularly for NLR readers.

National Law Review Cannabis TwitterFor hourly updates on the latest news about biotech, food & drug, and cannabis laws, regulations, and legislation, be sure to follow our Cannabis X (formerly Twitter) feed, and sign up for complimentary e-news bulletins.

Recent Biotechnology, Food & Drug Administration FDA News

Title
Publication Date Organization Sort descending
Feb
21
2018
No Judges Equals No Judgments: Administrative Confusion at USDA Morgan, Lewis & Bockius LLP
Feb
27
2018
FDA Issues Final Rule on Data Acceptance from Clinical Investigations for Medical Devices Morgan, Lewis & Bockius LLP
Feb
5
2014
West Virginia District Court Holds Reused Water and Condensate Are Not Resource Conservation and Recovery Act (RCRA) Solid or Hazardous Waste Morgan, Lewis & Bockius LLP
Aug
6
2014
Medical Device Update: FDA Issues Final Guidance on 510(k) Determinations, Use of “Split” Predicates Strongly Discouraged Morgan, Lewis & Bockius LLP
Jul
24
2015
FDA Proposes Rule and Releases Guidance on Third-Party Auditor Program to Expedite Qualified Foreign Food Imports Morgan, Lewis & Bockius LLP
Dec
11
2015
New York Sodium Labeling Requirements Go Into Effect Morgan, Lewis & Bockius LLP
Jan
15
2016
Groundbreaking Rule Encourages Gulf Coast Offshore Aquaculture Morgan, Lewis & Bockius LLP
Apr
21
2017
Congressional Committees Propose Restructuring of User Fees in Draft Language Morgan, Lewis & Bockius LLP
Mar
23
2018
Citizens Group Advocates Certain Limitations on Definitions of ‘Beef’ and ‘Meat’ Morgan, Lewis & Bockius LLP
Apr
9
2018
No Such Thing as Simple Food Labeling: Changes Ahead in 2018 Morgan, Lewis & Bockius LLP
May
22
2014
Federal Energy Regulatory Commission (FERC) Amends Open-Access Requirements for Interconnection Facilities Morgan, Lewis & Bockius LLP
Jan
24
2018
What Pharma Companies Need to Know about FDA’s New Draft IVD Guidance Morgan, Lewis & Bockius LLP
Feb
7
2018
More Than Peanuts Sentence of Food Company Officials Upheld Morgan, Lewis & Bockius LLP
Dec
29
2012
EPA Tightens Air Quality Standards for Fine Particles Morgan, Lewis & Bockius LLP
Mar
30
2018
Healthcare: What’s in the 2018 Omnibus Appropriations Law? Morgan, Lewis & Bockius LLP
Mar
24
2015
While FDA’s Proposed e-Cigarette Rule is Pending, FTC Mulls Enforcement Action Morgan, Lewis & Bockius LLP
Apr
10
2015
Farmers Markets, Roadside Stands, and CSA Programs Evade the Long Arm of the Law Morgan, Lewis & Bockius LLP
Nov
12
2015
FDA Fortification Policy – “Now With More Guidance!” Morgan, Lewis & Bockius LLP
Feb
17
2016
60-Day Rule Is Final: Assessing Your Organization’s Safeguards Morgan, Lewis & Bockius LLP
Apr
19
2016
FDA Active on Device Front for Q1 2016 Morgan, Lewis & Bockius LLP
May
27
2016
FDA Issues Final Rule on Food Defense Morgan, Lewis & Bockius LLP
Jul
28
2016
FDA Issues Draft Guidance as Part of Precision Medicine Initiative Morgan, Lewis & Bockius LLP
Jul
19
2017
Massachusetts SJC: Medical Marijuana Users May Be Safe from Employer Discrimination Morgan, Lewis & Bockius LLP
Dec
20
2013
Update: Last Obstacle Cleared for Mexican Energy Reform Morgan, Lewis & Bockius LLP
Mar
17
2014
Federal Energy Regulatory Commission (FERC) Directs Reliability Standards for Physical Security Morgan, Lewis & Bockius LLP
Jul
22
2014
Medical Device Update: FDA Medical Device Guidances Issued in 2014’s Second Quarter Morgan, Lewis & Bockius LLP
Aug
25
2014
Medical Device Update: FDA Issues Draft Guidance on Streamlined De Novo Classification Process Morgan, Lewis & Bockius LLP
Aug
10
2015
Practical Implications from Amarin Morgan, Lewis & Bockius LLP
 

NLR Logo

We collaborate with the world's leading lawyers to deliver news tailored for you. Sign Up to receive our free e-Newsbulletins

 

Sign Up for e-NewsBulletins