Biotech, Food, Drug

The food we eat and the medicine we put into our bodies are highly regulated by a variety of government agencies. In the United States by the Food and Drug Administration (FDA) and the United States Department of Agriculture (USDA) regulate the processes by which food makes its way to the grocery store and medicine is approved for consumer use.  As the science grows more complex behind the pharmaceutical and food industry, interpretation of the regulations in place is becoming more nuanced.  Overseas, these industries are regulated by a variety of agencies; for example, the Minister of Agriculture in Canada, Centre for Food Safety in Hong Kong, and the Committee of Environmental, Public Health and Food Safety (EU), are among the many governing-bodies which regulate biotechnology, food, and drugs throughout the world.

The National Law Review is your free online resource to agency news, emerging topics in food and drug, and the latest in biotechnology updates. From nanotechnologies being used in research, to regulations of imported foods coming into the US from overseas or the development of medical devices and drugs, readers can find expert legal analysis of the developments in the industry, as well as reports on changes within the agencies that regulate these industries. The National Law Review also covers topics related to licensing, Food Safety and Inspection Services (FSIS), food and beverage regulation in the US and worldwide, nutrition labeling, and country of origin labeling guidelines.

With recent legislation being passed throughout the US in relation to marijuana use, both for recreational and medicinal purposes, readers will also find up-to-date information, litigation, and news coming from this area of interest as well. Regulations in California for labeling and proper sales of marijuana, to use in different states, or internationally, as well as rules for promoting and advertising marijuana are also covered on the site. Additionally, the development and changing landscape of tobacco use to include vaping, and how e-cigarettes and vaping are regulated, is also covered by NLR authors.

Readers who are interested in food safety, inspection, imports into the US, and regulations, these topics are covered regularly on The National Law Review as well. New legislation from the FDA, USDA, Department of Agriculture, and international bodies, are covered on the site. If you are looking for details on new nutrition-labeling regulations or health risks of consuming certain imported foods, you will find these topics, and many more, on The National Law Review.

For hourly updates on the latest news about biotech, food & drug, and cannabis laws, regulations, and legislation, be sure to follow our Cannabis Twitter feed, and sign up for complimentary e-news bulletins.

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Jan
16
2014
Contaminated but Remediated Soil and Cortese Listing Does Not Compel Preparation of EIR (Environmental Impact Report) Sheppard, Mullin, Richter & Hampton LLP
Jun
12
2014
Proposed Health Information Technology Strategy Aims to Promote Innovation Sheppard, Mullin, Richter & Hampton LLP
Mar
30
2022
Movement On CMRE Act and MORE Act On Capitol Hill Sheppard, Mullin, Richter & Hampton LLP
Apr
20
2022
FDA Issues Untitled Letter to Bausch Health Companies for Misleading Statements Relating to DUOBRII™ Sheppard, Mullin, Richter & Hampton LLP
Jun
29
2022
Time Is Not Always Money: Ninth Circuit Holds That Pre-Employment Drug Testing Is Not Compensable Under California Law Sheppard, Mullin, Richter & Hampton LLP
Aug
8
2022
FDA Delays Enforcement of UDI Reporting Requirements for Consumer Health Products Sheppard, Mullin, Richter & Hampton LLP
Aug
30
2022
Charging for Investigational Drugs Under an IND Questions and Answers, Draft Guidance for Industry, August 2022 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
Feb
3
2020
Intellectual Property Outlook: Cases and Trends to Follow in 2020 — PART 2 Sheppard, Mullin, Richter & Hampton LLP
Jun
14
2023
FDA Issues Proposed Rule for Standardized and Accessible Patient Medication Information 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
Sep
7
2023
Context is Key: FDA Sends a Strong Message About Efficacy Claims Sheppard, Mullin, Richter & Hampton LLP
Sep
28
2023
A Second Chance to Win Your Government Healthcare Contract 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
Nov
8
2023
OIG General Compliance Program Guidance November 2023 Sheppard, Mullin, Richter & Hampton LLP
Dec
21
2023
Pharmaceutical Companies Have Rights if the Federal Government Seized their Patents 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
Mar
25
2024
PFAS in Food Packaging: The Beginning of the End? 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
19
2010
The FDA Transparency Initiative: Another One Way Street? 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
Oct
9
2013
Cloning Decision Could Lead to Copycat Litigation in the World of Racing Sheppard, Mullin, Richter & Hampton LLP
Oct
25
2021
AB-45: California Finally Welcomes Hemp Products To The Marketplace Sheppard, Mullin, Richter & Hampton LLP
Jan
7
2022
FDA Releases Guidance for Digital Health Tech Used in Clinical Investigations Sheppard, Mullin, Richter & Hampton LLP
Aug
12
2014
Sham Hatch-Waxman Infringement Suits And FDA Citizen Petitions; A Potential For New Liability For Innovators? Sheppard, Mullin, Richter & Hampton LLP
Aug
21
2014
Second Circuit Clarifies the Use of Legal Presumptions of Consumer Confusion and Injury in Certain Lanham Act Cases Sheppard, Mullin, Richter & Hampton LLP
Oct
14
2014
Device Advice: New Guidance From the FDA on Medical Devices and Cybersecurity 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
Dec
2
2022
Proposal to Overhaul Privacy Law Governing Substance Use Disorder Treatment Records Sheppard, Mullin, Richter & Hampton LLP
Dec
20
2022
Comment Period for “Healthy” Regulations Extended; But Consumer Class Actions Targeting “Health Halos” May Continue Sheppard, Mullin, Richter & Hampton LLP
May
25
2023
Florida Bans Offshoring of Certain Patient Information 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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