Administrative & Regulatory

Administrative agencies and changes in the area of regulatory law, are two areas of law which are regularly covered in the news media. And, because these areas of law change frequently, it is important to have the latest news which is available. The National Law Review covers the latest administrative and regulatory actions as they unfold. From appointment of new Administrative law judges (ALJs), to the appointment of the Officer of Management and Budget office in Mick Mulvaney, the National Law Review covers this, and other agency and regulatory news as it unfolds.

New regulations in tax-law, rulemaking decisions, the Securities and Exchange Commission (SEC), and the latest news in regulatory agendas, are reported on daily on NLR’s website. The adjudication and enforcement of regulatory agendas, new appointments to government offices and agencies, and news from the federal and state-level, is updated on the National Law Review daily. Readers can find information about new legislation, law-making, changes in government agencies, the appointment of new directors, and litigation involving administrative and regulatory news as it unfolds.

Anything encompassing new government regulations will also be found under the administrative and regulatory law section on The National Law Review. Regulations made by government agencies via the powers appointed to them by statutes or the Constitution are highly covered topics on the National Law Review as well. For visitors who want the latest information on the new administration which is heading the CFPB, to reading about new state regulations where they live, will find such topics covered on NLR.

Because news is unfolding on a regular basis, visitors want to read about the latest topics, areas of concern, and rulemaking which might affect them in the future. The National Law Review adds new content on a daily basis, meaning visitors will always have up-to-date legal analysis on regulations that may impact their business.

 

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Feb
14
2024
FDA Final Rule Harmonizes Medical Device Quality System Regulation with International Standard Greenberg Traurig, LLP
May
7
2024
FDA Finalizes Ag Water Rule Keller and Heckman LLP
Jul
31
2014
FDA Finalizes Appeals Guidance on Section 517A of the Food, Drug, and Cosmetic Act Covington & Burling LLP
Jan
25
2023
FDA Finalizes Cannabis Guidance Focusing on Clinical Research and Quality Considerations Nelson Mullins
Jan
11
2023
FDA Finalizes FSVP Guidance for Importers of Human and Animal Food Keller and Heckman LLP
Jul
7
2022
FDA Finalizes Guidance for Animal Food Facilities Keller and Heckman LLP
Oct
10
2014
FDA Finalizes Guidance for Management of Cybersecurity in Medical Devices Covington & Burling LLP
May
16
2022
FDA Finalizes Guidance on Reducing Microbial Hazards in Seed for Sprouting Keller and Heckman LLP
Jul
28
2014
FDA Finalizes Guidance on the Evaluation of 510(k) Substantial Equivalence Covington & Burling LLP
Jan
30
2023
FDA Finalizes Guidance to Prevent Unsafe Contamination of Animal Feed from Drug Carryover Keller and Heckman LLP
Aug
15
2023
FDA Finalizes Informed Consent Guidance for Drug and Medical Device Clinical Investigations Nelson Mullins
Aug
2
2022
FDA Finalizes NAC Enforcement Discretion Guidance Keller and Heckman LLP
Dec
11
2020
FDA Finalizes New Guidance for Animal Food Additive Petitions and GRAS Notice Reviews Keller and Heckman LLP
Mar
1
2024
FDA Finalizes Revised Medical Device Quality System Requirements, Issues Remote Regulatory Assessments Guidance McDermott Will & Emery
May
6
2024
FDA Finalizes Rule Regulating Laboratory Developed Tests Polsinelli PC
Feb
26
2019
FDA Finalizes Two Guidance Documents Regarding Regenerative Medicine Therapies Epstein Becker & Green, P.C.
Sep
13
2018
FDA Finalizes Voluntary Malfunction Summary Reporting Program to Streamline Manufacturer Reporting Covington & Burling LLP
Mar
15
2013
FDA Flexes Its FSMA Muscles, Initiates Mandatory Recall Morgan, Lewis & Bockius LLP
Sep
11
2014
FDA Focuses on Sex-Specific Data in Medical Device Clinical Trials Covington & Burling LLP
Nov
5
2013
FDA Food Safety Modernization Act (FSMA) Extension of Comment Period Announced McDermott Will & Emery
Jun
10
2019
FDA Forms PFAS Working Group Keller and Heckman LLP
Mar
11
2020
FDA Gives a CBD Update: Spoiler Alert! It’s More or Less the Same Old News Mintz
Jun
30
2014
FDA Gives an Inch, But Only an Inch, on Use of Social Media to Promote Drugs and Devices Barnes & Thornburg LLP
May
14
2020
FDA Gives Guidance on Reporting Medical Device Shortages Faegre Drinker
Mar
16
2020
FDA Grants COVID-19 Diagnostic Emergency Use Authorizations, And Other Recent FDA Actions With to Address COVID-19 Sheppard, Mullin, Richter & Hampton LLP
Jul
18
2014
FDA Grapples with Nanotechnology Covington & Burling LLP
Jul
16
2022
FDA Greenlights Pharmacists to Prescribe COVID-19 Drug Paxlovid Epstein Becker & Green, P.C.
Aug
6
2020
FDA Greenlights Updates to the Purple Book Database Mintz
May
20
2019
FDA Greenlights Use of “Potassium Chloride Salt” as an Alternative Name for “Potassium Chloride” in Food Labeling Keller and Heckman LLP
Sep
25
2019
FDA Guidance Clarifies HDE Program Review Epstein Becker & Green, P.C.
Dec
7
2021
FDA Guidance on China Food Facility Registration Keller and Heckman LLP
Nov
2
2021
FDA Guidance: Temporary Marketing Permits Keller and Heckman LLP
Dec
21
2020
FDA Guidance: Use of “Potassium Salt” as an Alternate Name for “Potassium Chloride” in Food Labeling Keller and Heckman LLP
Sep
6
2019
FDA Highlights Best Practices to Prevent Tampering and Intentional Adulteration of Food and Cosmetics Keller and Heckman LLP
May
31
2019
FDA Holds First Public Hearing on CBD Regulation Steptoe & Johnson PLLC
 

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