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
Sep
29
2016
FDA Issues Draft Guidance on Risk Evaluation and Mitigation Strategy (REMS) Determinations McDermott Will & Emery
Sep
29
2016
Fruit Labeling Accuracy Act of 2016 Would Prohibit Added Sugars Labeling for Naturally Tart Fruits Keller and Heckman LLP
Sep
28
2016
International Organization for Standardization Publishes Standard for Compilation and Description of Sample Preparation and Dosing Methods for Engineered and Manufactured Nanomaterials Bergeson & Campbell, P.C.
Sep
28
2016
FDA Updates Food Facility Registration Product Categories Keller and Heckman LLP
Sep
28
2016
French Pilot on Mandatory Country of Origin Labelling (COOL) for Dairy and Meat in Processed Foods Covington & Burling LLP
Sep
27
2016
The Hullabaloo about Healthy: FDA Formally Seeks to Redefine “Healthy” Keller and Heckman LLP
Sep
27
2016
FDA Holding its First Public Meeting on Drug Product Identification Requirements in October Mintz
Sep
27
2016
Drug Company Accused of Price-Gouging Has Developed Deep Capitol Network Since 2010 MapLight
Sep
26
2016
Revisions to Industry Guidance Regarding FDA Health Document Submission Requirements for Tobacco Products Keller and Heckman LLP
Sep
26
2016
Vanda v. Roxane Labs. – Are Two Natural Laws Better Than One? Schwegman, Lundberg & Woessner, P.A.
Sep
26
2016
Soda Showdown: Beverage Industry Takes Philadelphia to Court Keller and Heckman LLP
Sep
26
2016
Review of International Regulation of Social Media Promotions at the 2016 RAPS Conference Mintz
Sep
25
2016
USDA Announces Assistance for Milk Producers Varnum LLP
Sep
25
2016
GMO Labeling Bill Signed into Law Varnum LLP
Sep
24
2016
Michigan Animal Remedies Program Ending this Fall Varnum LLP
Sep
23
2016
Comments Due November 1, 2016 on Proposed Update to Framework for Biotechnology Regulation Beveridge & Diamond PC
Sep
23
2016
Organic Melee: USDA Loses Latest Round in Legal Challenge Over Synthetics in Organic Production Keller and Heckman LLP
Sep
23
2016
Naval Air Station Successfully Tests Flight With 100 Percent Advanced Biofuel Bergeson & Campbell, P.C.
Sep
22
2016
Food Safety and Inspection Service Issues New Directive Addressing HPAI and Agro-Terrorism Keller and Heckman LLP
Sep
22
2016
GMO Food Labeling And CRISPR-modified Foods Foley & Lardner LLP
Sep
21
2016
White House Releases Proposed Update to the Coordinated Framework and National Strategy for Modernizing the Regulatory System for Biotechnology Products Bergeson & Campbell, P.C.
Sep
21
2016
Administration’s Biotechnology Working Group Updates Coordinated Framework & Unveils National Strategy Mintz
Sep
21
2016
EPA Researches How Sunscreens Containing Engineered Nanomaterials Might Change When Exposed to Chemicals in Pool Water Bergeson & Campbell, P.C.
Sep
21
2016
Catfish Controversy Continues: Lawmakers Push To Upend USDA Inspection Program Keller and Heckman LLP
Sep
20
2016
California Environmental Protection Agency's Office of Environmental Health Hazard Assessment Issues Notice of Intent to List PFOA and PFOS Bergeson & Campbell, P.C.
Sep
20
2016
FDA Extends Deadline for Removal of NDC and NHRIC Numbers from Device Labeling and Packaging McDermott Will & Emery
Sep
20
2016
FDA Announces Public Hearing on Off-Label Communications; Registration Deadline October 19, 2016 McDermott Will & Emery
Sep
20
2016
Antibiotic Ire: Groups Petition FDA to Limit Antibiotic Use in Food Animals Keller and Heckman LLP
 

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