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
Mar
25
2022
Judge Questions Plausibility of “0g Total Sugar” Claim Keller and Heckman LLP
Jan
3
2019
FDA, USDA Impacted by Lapse in Government Funding Keller and Heckman LLP
Apr
11
2022
FDA Completes Review of GE Canola Seeds After Response to Last Year’s Inadvertent Release Keller and Heckman LLP
Apr
21
2022
CSPI Criticizes FDA Allergen Guidance Keller and Heckman LLP
Apr
28
2022
India: Another Booming Market for Alternative Proteins in Asia Keller and Heckman LLP
Jan
25
2019
New Guidance Document Reviews Global Packaging Materials Definitions Keller and Heckman LLP
Feb
1
2019
Cannabis Quick Hits Keller and Heckman LLP
Feb
22
2019
FDA Adds Ten New Substances to its Inventory of Effective FCS Notifications Keller and Heckman LLP
Feb
28
2019
EFSA Report Indicates Antimicrobial Resistance in EU Is Increasing Keller and Heckman LLP
Mar
5
2019
FDA Takes New Steps to Curtail Youth Access to Tobacco Products and E-Cigarettes Keller and Heckman LLP
Jun
17
2022
HELP Committee Approves Bill to Address Infant Formula Shortage Keller and Heckman LLP
Mar
11
2019
FSIS Issues Draft Guidance to Industry for Responding to Consumer Complaints Keller and Heckman LLP
Mar
15
2019
HHS and USDA Announce 2020 Dietary Guidelines Topics and Advisory Committee Meeting Keller and Heckman LLP
Apr
5
2019
FDA Releases Heavy Metal Test Results in Kratom Keller and Heckman LLP
Jul
22
2022
FSIS Puts Cell-Cultured Meat Labeling Regulations On Hold Keller and Heckman LLP
May
6
2019
Canada Expands Use of Fines for Food Safety Noncompliance Keller and Heckman LLP
May
10
2019
Product Recalls Decline Across All Industries in Q1 2019 Keller and Heckman LLP
May
22
2019
Louisiana Bill Would Require Shrimp and Crawfish Country Of Origin Labeling on Restaurant Menus Keller and Heckman LLP
May
28
2019
USDA Updates FAQs Regarding BE Labeling Keller and Heckman LLP
Jun
4
2019
Is FDA Clearance Needed to Import Plastic and Paper Cups, Utensils, and Takeout Containers? Keller and Heckman LLP
Jun
7
2019
USDA Removes Standard for “Jambalaya” Keller and Heckman LLP
Oct
26
2022
Baby Food Lawsuit Dismissed for Relying on “Inferential Leaps” Keller and Heckman LLP
Jun
25
2019
FDA Issues Draft Guidance on Reducing Microbial Hazards in Seed for Sprouting Keller and Heckman LLP
Jul
2
2019
EPA Releases Draft Risk Evaluations for Two More of the "First Ten Chemicals" - 1,4 Dioxane and Cyclic Aliphatic Bromide Cluster (HBCD) Keller and Heckman LLP
Dec
7
2022
External Evaluation of FDA’s Human Foods Program Published Keller and Heckman LLP
Jul
22
2019
FSIS Publishes Tips for Label Application Submissions Amidst Evaluation Backlogs Keller and Heckman LLP
Dec
22
2022
Omnibus Bill for Fiscal Year 2023 (H.R. 2617) – Cosmetics Summary Keller and Heckman LLP
Aug
8
2019
Inspections Begin Under FDA’s Produce Safety Rule Keller and Heckman LLP
 

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