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 ascending
Oct
18
2023
DOJ's Consumer Protection Branch Continues Civil Enforcement Against Pharmacies, Pharmacists for Opioid Dispensing Barnes & Thornburg LLP
Aug
22
2016
After 19 Years, FDA Issues Final Rule on GRAS Notices Barnes & Thornburg LLP
Aug
26
2016
FDA Updates Benefit-Risk Determinations for New Medical Devices Barnes & Thornburg LLP
Oct
12
2016
Effective Immediately: FDA Issues Guidance on Use of ‘Healthy’ in Food Labeling Barnes & Thornburg LLP
Apr
19
2024
HHS-OIG Highlights Anti-Fraud Safeguards for Patient Assistance Programs Backed Mainly By Drug Manufacturers Barnes & Thornburg LLP
Jul
6
2017
Ohio Budget Update- July 6, 2017 Barnes & Thornburg LLP
Aug
23
2017
FDA Issues Guidance on Qualification of Medical Device Development Tools Alert Barnes & Thornburg LLP
Dec
15
2012
Michigan Lame Duck Legislative Changes to Environmental Cleanup of Contaminated Sites and Leaking Underground Storage Tanks Barnes & Thornburg LLP
Oct
11
2018
FDA Issues Draft Guidance on Expanding Special 510(K) Program Barnes & Thornburg LLP
Jan
11
2014
EPA (Environmental Protection Agency) Publishes Proposed Rule to Cap Carbon Emissions from New Power Plants Barnes & Thornburg LLP
Jun
16
2014
FDA Issues Draft Guidance on Distributing Favorable New Risk Information for Drugs Barnes & Thornburg LLP
Jul
18
2014
Food and Drug Administration (FDA) Releases Draft Guidance on Benefit and Risk Analysis for 510(k)s Barnes & Thornburg LLP
Sep
21
2015
FDA Publishes Final Rule on Preventive Controls for Human Food Barnes & Thornburg LLP
Aug
27
2016
FDA Extends Compliance Dates for Certain Final Rules Under the Food Safety Modernization Act Barnes & Thornburg LLP
Jan
4
2017
FDA Issues Final Guidance on Postmarket Management of Cybersecurity in Medical Devices Barnes & Thornburg LLP
Jan
25
2013
Fine Particle Emissions Rules Remanded- Stricter Clean Air Regulations for Nonattainment Areas Will Follow Barnes & Thornburg LLP
Sep
27
2021
Tough Yardage Barnes & Thornburg LLP
Sep
13
2013
“Innocent” Purchasers Beware: U.S. EPA Withdraws New Environmental Site Assessment Standard Barnes & Thornburg LLP
Nov
5
2018
FDA Issues Draft Guidance Documents on New Nutrition Facts Label Barnes & Thornburg LLP
Jan
27
2022
New Tools in the Fight Against Counterfeit Pharmaceuticals Barnes & Thornburg LLP
Mar
14
2019
IPAs and ILWU? Craft Brewery Unionized For The First Time In The U.S. Barnes & Thornburg LLP
Oct
6
2014
FDA Issues Final Guidance on Cybersecurity for Medical Devices Barnes & Thornburg LLP
Jun
20
2019
Bipartisan Senate Efforts to Mandate Agencies Address Growing PFAS Crisis Barnes & Thornburg LLP
Feb
17
2016
CMS Relaxes 60-day Overpayment “Look Back” Period for Medicare Providers Barnes & Thornburg LLP
Apr
3
2017
Warning: California Takes Aim at Food and Beverage Industry Barnes & Thornburg LLP
Apr
13
2017
FDA Publishes List of Class I Devices Exempted From 510(k) Process Barnes & Thornburg LLP
Nov
1
2017
FDA Updates De Novo Medical Device Classification Process Barnes & Thornburg LLP
Oct
29
2018
Two Food Safety Modernization Act Draft Guidance Documents Issued by FDA for Farmers, Food Processors Barnes & Thornburg LLP
 

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