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
Aug
12
2016
Draft Guidance on 510(k)s: FDA Issues Guidance on When Medical Device Modifications Require a New 510(k) and on Software Changes [INFOGRAPHICS] Barnes & Thornburg LLP
Aug
12
2016
German BfR Recommends More Studies on Epoxide Resin Coatings for Oily Foods Keller and Heckman LLP
Aug
11
2016
DEA Declines to Change Stance on Marijuana but Opens Door to Federally Sanctioned Marijuana Research McDermott Will & Emery
Aug
11
2016
DEA Denies Petitions To Reschedule Marijuana But Will Authorize More Marijuana Manufacturing To Foster Research Jackson Lewis P.C.
Aug
11
2016
Supplement Spotlight: FDA Revises Non-Dietary Ingredients Draft Guidance Keller and Heckman LLP
Aug
10
2016
Ohio’s Employer-Friendly Medical Marijuana Law Takes Effect September 6, 2016 Jackson Lewis P.C.
Aug
10
2016
FDA Publishes Long-Awaited Draft Guidance on 510(k) Requirements for Modified Devices McDermott Will & Emery
Aug
10
2016
San Francisco Soda Warning Free Speech Suit Keller and Heckman LLP
Aug
9
2016
Petition Denied for Johnson & Johnson and DePuy Multidistrict Litigation Appeal Stark & Stark
Aug
9
2016
Labeling Requirement: FDA Publishes Nutrition Facts FAQs Keller and Heckman LLP
Aug
9
2016
AbbVie Sues Amgen On 10 Of 100 Humira Patents Foley & Lardner LLP
Aug
8
2016
DeCoster Decision—What Food and Beverage Companies Need To Know Katten
Aug
8
2016
Consumer Protection: Let’s Talc About Baby Powder ArentFox Schiff LLP
Aug
8
2016
GM Labeling, Vending Machine Label: Food Regulatory News Round-up Keller and Heckman LLP
Aug
8
2016
FDA Finalizes Guidance on Low-Risk Devices Foley & Lardner LLP
Aug
5
2016
FDA Finalizes General Wellness Guidance Covington & Burling LLP
Aug
5
2016
Father and Son Food Company Executives Sentenced to Prison for Salmonella Outbreak Keller and Heckman LLP
Aug
5
2016
President Signs Bill Creating National GMO Food Disclosure Standard Bergeson & Campbell, P.C.
Aug
4
2016
First-Ever Federal Labeling Requirements for Bioengineered Foods Signed Into Law Beveridge & Diamond PC
Aug
4
2016
FDA FY 2017 Medical Device User Fees Announced Covington & Burling LLP
Aug
4
2016
FDA Issues Guidance on Use of Public Human Genetic Variant Databases and Their Use in Personalized Medicine Foley & Lardner LLP
Aug
4
2016
OSHA Blogs on How to Protect Workers from Zika Exposure Holland & Hart LLP
Aug
3
2016
FDA Finalizes Guidance on Low Risk General Wellness Devices McDermott Will & Emery
Aug
3
2016
Italian Medicines Agency Publishes New Concept Paper on Biosimilars Covington & Burling LLP
Aug
2
2016
FDA Publishes Draft Guidance on Codevelopment of Companion Diagnostics Covington & Burling LLP
Aug
2
2016
White Paper Describes Nanotechnology-Inspired Grand Challenge for Future Computing Bergeson & Campbell, P.C.
Aug
2
2016
States’ Efforts for Drug Price Transparency Stymied by the Pharmaceutical Industry Mintz
Aug
2
2016
Mid-Year Medicare 340B Drug Pricing Program Update Foley & Lardner LLP
 

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