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
May
20
2016
FDA Final Rule Alert: Revised Nutrition Facts and RACCs Keller and Heckman LLP
May
20
2016
FDA Issues Draft Guidance for Qualified Facilities under the FSMA Preventive Controls Rules Morgan, Lewis & Bockius LLP
May
20
2016
The FDA’s New E-Cigarette Rule: Regulating this Hypothetical Risk May Do More Harm than Good Dinsmore & Shohl LLP
May
19
2016
Antitrust: Third Circuit Provides Guidance on Loyalty Discounts ArentFox Schiff LLP
May
19
2016
San Francisco Sugar Lawsuit Shutdown: Beverages Keller and Heckman LLP
May
19
2016
FDA Issues “Leapfrog” Draft Guidance for 3D Printing of Medical Devices Morgan, Lewis & Bockius LLP
May
19
2016
USPTO 101 Guidance: Microneedles Versus Prosthetic Devices Foley & Lardner LLP
May
18
2016
Vermont Enforcement of Genetically Modified Foods Bulletin: Food Law Keller and Heckman LLP
May
17
2016
FDA Issues Draft Guidance on Additive Manufacturing Including 3D Printing Barnes & Thornburg LLP
May
17
2016
Pet Jerky Update: Food Law Keller and Heckman LLP
May
17
2016
Amgen And Sandoz Do Biosimilar Patent Dance Over Neulasta Foley & Lardner LLP
May
16
2016
FSMA Guidance: Qualified Facility Q&A Keller and Heckman LLP
May
16
2016
Discussions Continue Regarding Federal Labeling Standards for Genetically Modified Organisms Squire Patton Boggs (US) LLP
May
16
2016
Indian Patent Office's Patent to Gilead’s Sovaldi Challenged at Delhi High Court Michael Best & Friedrich LLP
May
13
2016
E-Cigarette Poisoning in Children on the Rise Stark & Stark
May
13
2016
USDA Convenes Public Meeting Of The Advisory Committee On Biotechnology And 21st Century Agriculture Bergeson & Campbell, P.C.
May
13
2016
3-D Printing and the Regulatory Future of Home Remedies: Pharma to Table New York University School of Law
May
12
2016
Just as Comment Period for “Natural” Ends, FDA Announces Intent to Re-Examine What It Means to Be a “Healthy” Food Mintz
May
12
2016
European Parliament Committee Calls for Further Harmonization in the Area of Food-Contact Materials Keller and Heckman LLP
May
12
2016
Brexit – What are Implications for UK Chemical Regulatory Law and Policy? Squire Patton Boggs (US) LLP
May
12
2016
FDA Will Reconsider Meaning of “Healthy” Morgan, Lewis & Bockius LLP
May
12
2016
Pennsylvania Employee Proceeds With Invasion of Privacy Claim Arising Out Of Positive Drug Test Result Jackson Lewis P.C.
May
12
2016
Medical Food FAQs: Food Law FDA Regulation Keller and Heckman LLP
May
12
2016
Initial Xarelto Trials Scheduled for 2017 Stark & Stark
May
12
2016
New USPTO Guidance On Patent Eligibility Of Natural Products Foley & Lardner LLP
May
11
2016
Diet Data: FDA Survey Findings Keller and Heckman LLP
May
11
2016
Australia Addresses Nanomaterials in Third NICNAS Reforms Consultation Paper Bergeson & Campbell, P.C.
May
10
2016
FDA Hones in on Definition of “Healthy”: Food Law Keller and Heckman LLP
 

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