Biotech, Food & Drug

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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
Mar
15
2017
Foreign Investment Under Trump Administration Sheppard, Mullin, Richter & Hampton LLP
Mar
15
2017
More Calls for a National Food Safety Strategy Keller and Heckman LLP
Mar
15
2017
FDA Published List of Class II Devices to be Exempt From 510(K) Process Barnes & Thornburg LLP
Mar
15
2017
E-Cigs are Gateway to Cigarette Smoking Stark & Stark
Mar
14
2017
User Fee Acts in Health Care: Let the 2017 “UFA” Games Begin! Mintz
Mar
14
2017
FSIS Increases Beef Import Inspection From Certain Countries: USDA’s Food Safety and Inspection Service Keller and Heckman LLP
Mar
13
2017
THE LATEST: Losing Bidder for Pharmaceutical Triggers FTC Investigation, Fix, and $100 Million Fine in Non-HSR-Reportable Transaction McDermott Will & Emery
Mar
13
2017
FDA Talks “Healthy” with Industry Keller and Heckman LLP
Mar
13
2017
Sonny Perdue One Step Closer to Agriculture Secretary Squire Patton Boggs (US) LLP
Mar
13
2017
NAS Issues Report on Preparing for Future Products of Biotechnology: National Academies of Sciences, Engineering, and Medicine Bergeson & Campbell, P.C.
Mar
13
2017
Medical Devices, Trade Talks, Medicine Manufacturing: EU Public Policy March 13 Update Squire Patton Boggs (US) LLP
Mar
10
2017
U.S. Senators Seek Clarification From Department of Justice Regarding Federal Marijuana Enforcement Priorities Jackson Lewis P.C.
Mar
10
2017
Honey Groups Urge FDA to Drop “Added Sugars” Labeling Requirement Keller and Heckman LLP
Mar
10
2017
European NanoSafety Cluster Publishes 2017 Research Regulatory Roadmap Bergeson & Campbell, P.C.
Mar
9
2017
Green Groups Petition EPA to Overhaul CAFO Regulations Michael Best & Friedrich LLP
Mar
9
2017
DOE Publishes Report On Biorefinery Optimization Workshop Bergeson & Campbell, P.C.
Mar
9
2017
USDA Delays Place Federal GMO Food Disclosure Rules in Limbo Keller and Heckman LLP
Mar
8
2017
Finally! FDA Issues Draft Guidance on Interchangeable Biosimilars Katten
Mar
8
2017
Nutrition Facts: Health Groups Call For FDA to Keep July 2018 Compliance Date Keller and Heckman LLP
Mar
8
2017
The Regulation of Printing Inks in the European Union Keller and Heckman LLP
Mar
7
2017
Proposed Regulation in Texas on Name and Address Labeling for Malt Beverages McDermott Will & Emery
Mar
7
2017
EPA Denies TSCA Section 21 Petition on Fluoride Chemicals in Drinking Water; Provides Response to Petition Bergeson & Campbell, P.C.
Mar
7
2017
California Bill Requiring Soda Warning Labels Introduced in California Senate Again Keller and Heckman LLP
Mar
7
2017
Will Avastin Biosimilar Patent Dance Go On? Foley & Lardner LLP
Mar
6
2017
Xarelto Bleeding Lawsuits Mount Against Johnson & Johnson Rosenfeld Injury Lawyers
Mar
6
2017
WHO Publishes First Ever List of Antibiotic Resistant “Priority Pathogens” Keller and Heckman LLP
Mar
3
2017
DOE Launches Consortium To Tackle Catalysis Challenges Bergeson & Campbell, P.C.
Mar
3
2017
DOE Announces Recipients Of $5.9 Million In Funding For CO2 Utilization Strategies Bergeson & Campbell, P.C.
 

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