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
Oct
14
2014
Device Advice: New Guidance From the FDA on Medical Devices and Cybersecurity Sheppard, Mullin, Richter & Hampton LLP
Jun
27
2022
PFAS Regulations Could Open Floodgates to Prop 65 Enforcement – Assess & Manage Your Exposure Now Sheppard, Mullin, Richter & Hampton LLP
Feb
18
2015
FDA Issues Guidance for Mobile Medical Applications: What Will be Subject to FDA Oversight and Enforcement? Sheppard, Mullin, Richter & Hampton LLP
Jul
17
2019
Don’t Spill Your Trade Secrets: Protecting Your Competitive Advantage in the Food and Beverage Industry (Part 1 of 2) Sheppard, Mullin, Richter & Hampton LLP
Jul
23
2019
Don’t Spill Your Trade Secrets: Protecting Your Competitive Advantage in the Food and Beverage Industry (Part 2 of 2) Sheppard, Mullin, Richter & Hampton LLP
Mar
29
2023
FDA Issues First Untitled Letter of the Year to HCT/P Manufacturer Sheppard, Mullin, Richter & Hampton LLP
Feb
3
2020
Intellectual Property Outlook: Cases and Trends to Follow in 2020 — PART 2 Sheppard, Mullin, Richter & Hampton LLP
Mar
11
2020
FDA Postpones Ex-US Facility Inspections Sheppard, Mullin, Richter & Hampton LLP
Apr
14
2020
Update: Key FDA Actions for COVID-19 Devices and Therapies (as of April 14) Sheppard, Mullin, Richter & Hampton LLP
Oct
17
2023
United Cannabis Corporation v. Pure Hemp Collective Inc. Sheppard, Mullin, Richter & Hampton LLP
Oct
25
2023
Connecticut Follows in the Footsteps of Other Jurisdictions Requiring Registration of Pharmaceutical Representatives Sheppard, Mullin, Richter & Hampton LLP
May
27
2020
Impact Of COVID-19 On Illinois Cannabis Contracts — Do Force Majeure Clauses Provide A Defense To Non-Performance Sheppard, Mullin, Richter & Hampton LLP
Aug
19
2020
Using ADR for Cannabis Disputes Sheppard, Mullin, Richter & Hampton LLP
Sep
25
2020
FDA Update: The Latest on Vaccine Development, Inspections, and Conducting Clinical Trials During Covid-19 Sheppard, Mullin, Richter & Hampton LLP
Nov
2
2020
The U.S. Court of Appeals Denies Rehearing on Cuts to 340B Drug Pricing Program Sheppard, Mullin, Richter & Hampton LLP
Jul
24
2010
FDA's Regulation of Laboratory Developed Tests (LDTs) - Changes on Horizon? Sheppard, Mullin, Richter & Hampton LLP
Nov
7
2010
United States Weighs in on Myriad Genetics Case Sheppard, Mullin, Richter & Hampton LLP
Jun
21
2013
Failure To Separately Notice Consideration Of California Environmental Quality Act (CEQA) Document Violates Brown Act Sheppard, Mullin, Richter & Hampton LLP
Sep
28
2021
Nota Bene Episode 145: Tuna Sustainability: A Model Bigger than its Niche with ISSF President Susan Jackson [PODCAST] Sheppard, Mullin, Richter & Hampton LLP
Oct
18
2021
California Broadens Security and Breach Laws, Includes Genetic Data Sheppard, Mullin, Richter & Hampton LLP
Oct
9
2013
Cloning Decision Could Lead to Copycat Litigation in the World of Racing Sheppard, Mullin, Richter & Hampton LLP
Jan
4
2022
Cannabis Legislation Year-in-Review Sheppard, Mullin, Richter & Hampton LLP
Apr
18
2022
China Proposed Draft Implementing Rules for Human Genetic Resources Management Sheppard, Mullin, Richter & Hampton LLP
May
19
2022
FDA White Paper Signals Shift to Performance-Based Reviews of Mature Quality Systems Sheppard, Mullin, Richter & Hampton LLP
Jul
8
2022
New Population-Based Option for the Maryland Primary Care Program in 2023 Sheppard, Mullin, Richter & Hampton LLP
Oct
7
2022
California Expands Employees’ Right to Off-Duty Cannabis Use Sheppard, Mullin, Richter & Hampton LLP
Oct
12
2015
Next Rx: New Medicare Part D Initiative Advances Role of Medication Management in Reform Sheppard, Mullin, Richter & Hampton LLP
Feb
21
2020
California Update: New QR Code Certificate Requirements, Uptick in Enforcement Actions, and the Future of California’s Cannabis Regulators Sheppard, Mullin, Richter & Hampton LLP
 

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