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
Jan
4
2016
Happy New(s) Year re: Food and Drug Law Keller and Heckman LLP
Jan
4
2016
Alcohol and Tobacco Tax and Trade Bureau (TTB) Publishes Projected Regulatory Agenda as Part of Government’s Unified Agenda McDermott Will & Emery
Jan
4
2016
FDA Releases Guidance to Assist Development of Advanced Technology to Modernize Pharmaceutical Manufacturing Epstein Becker & Green, P.C.
Jan
4
2016
Did PTAB Dose AIA Poison Pill Incorrectly Against Premium Genetics? Foley & Lardner LLP
Jan
3
2016
Tariff Trouble - Country of Origin Labeling Keller and Heckman LLP
Jan
1
2016
Organic Challenges in California OK Keller and Heckman LLP
Dec
31
2015
Federal Food Waste Foray Keller and Heckman LLP
Dec
31
2015
Chicken Out - FDA approves Transgenic Chicken Keller and Heckman LLP
Dec
31
2015
Antibiotic Ascent re: Promoting Growth or Feed Efficiency in Food-producing Animals Keller and Heckman LLP
Dec
31
2015
Poultry Practice Points Keller and Heckman LLP
Dec
31
2015
Eye on the EU: EFSA Data Warehouse Keller and Heckman LLP
Dec
31
2015
USDA Beefs Up Product Tracing Keller and Heckman LLP
Dec
31
2015
Altaire Pharmaceuticals v. Paragon Bioteck: Decision Denying Institution In Part Where Petitioner Had Not Alleged Unpatentability With Sufficient Particularlity Faegre Drinker
Dec
31
2015
Nanomaterials Reporting Requirement Proposed by Swedish Chemicals Agency Keller and Heckman LLP
Dec
30
2015
California Lists an Aloe Vera extract and Goldenseal Root Powder under Prop 65 Keller and Heckman LLP
Dec
30
2015
Omnibus Edition re: Food & Drug Keller and Heckman LLP
Dec
30
2015
Funding for FDA’s FCN Program Included in Consolidated Appropriations Act Keller and Heckman LLP
Dec
30
2015
Tomato Toss re: Food & Drug Keller and Heckman LLP
Dec
30
2015
Laboratories – 2015 Year in Review [VIDEO] Mintz
Dec
30
2015
TTAB Finds MEAT CANDY to be Too Sweet Sterne, Kessler, Goldstein & Fox P.L.L.C.
Dec
30
2015
Current State of Data Protection and Exclusivity in Russia Michael Best & Friedrich LLP
Dec
30
2015
Getting Past Gatekeeper: “No Shoes, No Shirt, No Service” re: Admissibility of Expert Opinions IMS Legal Strategies
Dec
30
2015
European Court of Justice Rules Scottish Law Establishing Minimum Unit Pricing for Alcoholic Drinks May Violate EU Law McDermott Will & Emery
Dec
29
2015
Federal Motor Carrier Safety Administration Slashes Random Drug Testing Percentage Rate for 2016 Jackson Lewis P.C.
Dec
29
2015
Don't Blame Patents For High Drug Prices
Dec
24
2015
Propriety of Certificate of Correction Requires Assessment of Teachings of Specification as Whole McDermott Will & Emery
Dec
22
2015
Comprehensive Amendments of German Drug Laws upcoming Covington & Burling LLP
Dec
22
2015
FDA Announces Commitment to Medical Device Single Audit Program (MDSAP) Squire Patton Boggs (US) LLP
 

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