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 Sort descending
Sep
29
2023
FDA’s Updated HARPC Draft Guidance Addresses Concerns Regarding Industry Approach to Sesame Keller and Heckman LLP
Oct
10
2023
EU Proposal for a Regulation on Packaging and Packaging Waste – the Highlights Keller and Heckman LLP
Oct
18
2016
New Data on BPA Do Not Support Changing Tolerable Daily Intake, Says European Food Safety Authority Keller and Heckman LLP
Oct
25
2016
Federal Trade Commission Complaint Targets Egg Supplier Ads Keller and Heckman LLP
Nov
14
2016
USDA Proposes Changes to Process Verified Program for Marketing Claims Keller and Heckman LLP
Jul
2
2020
Chinese Food Industry Proposes the First Group Standard for Plant-Based Meat Keller and Heckman LLP
Nov
3
2023
Proposed Amendments to Prop 65’s Warning Requirements Keller and Heckman LLP
Nov
30
2016
FDA Menu Labeling Update Keller and Heckman LLP
Jul
8
2020
China Places a Higher Priority on Food Nutrition Keller and Heckman LLP
Dec
8
2016
FDA Issues Guidance for Industry on Model Accreditation Standards for Third-Party Certification Bodies Keller and Heckman LLP
Dec
13
2016
New EU Guidance Documents on Authorization of Novel and Traditional Foods Now Available Keller and Heckman LLP
Jul
16
2020
USDA’s Proposed Rule Strengthens the Enforcement and Oversight of Organics Keller and Heckman LLP
Jan
9
2017
FDA Extends Comment Period for Information and Draft Guidance on Fiber on Nutrition Facts Label Keller and Heckman LLP
Jan
20
2017
Toxicity Data on Chemicals Found in Food Now Available on European Food Safety Authority Website Keller and Heckman LLP
Dec
18
2023
The ‘One Substance, One Assessment Package’: Implications, Upcoming Pilot Project, Impact on EFSA Keller and Heckman LLP
Jan
25
2017
Packaging Requirements Included in Canada’s SFCA Proposed Implementing Regulations Keller and Heckman LLP
Jan
30
2017
Nonprofit Group Tells FDA High-Sugar Foods Should Not Bear “Healthy” Claims Keller and Heckman LLP
Sep
1
2020
OEHHA Releases Report Assessing Potential Neurobehavioral Effects of Synthetic Food Dyes in Children Keller and Heckman LLP
Jan
3
2024
FDA Supplements Response to D-Tagatose Petition Keller and Heckman LLP
Jan
5
2024
Texas Urges Federal Court to Toss Tofurky Challenge of Labeling Law Keller and Heckman LLP
Feb
9
2017
USDA Delays Final Rule on Organic Livestock and Poultry Practices Keller and Heckman LLP
Sep
21
2020
Germany Notifies Updated Version of its Draft Mineral Oil Ordinance to the EC Keller and Heckman LLP
Jan
17
2024
California's Proposition 65: A Regulatory Conundrum Keller and Heckman LLP
Mar
3
2017
FSIS Extends Comment Period for Updated Nutrition Labeling Requirements Keller and Heckman LLP
Jan
31
2024
FDA Revises Draft HARPC Guidance Keller and Heckman LLP
Mar
10
2017
Honey Groups Urge FDA to Drop “Added Sugars” Labeling Requirement Keller and Heckman LLP
Mar
16
2017
Food Labeling: Natural Challenge Stayed Keller and Heckman LLP
Oct
20
2020
FDA Announces Establishment of U.S. Agent Voluntary Identification System Keller and Heckman LLP
 

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