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On Nov. 8, the National Labor Relations Board (NLRB) issued yet another decision upending nearly 40 years of prior precedent.

On Dec. 17, 2010, President Obama signed into law the Tax Relief, Unemployment Insurance Reauthorization, and Job Creation Act of 2010 (the 2010 Tax Act), a multi-billion dollar tax cut package that generally extends the Bush income tax cuts for individuals and the lower capital gain/dividend tax rates for all taxpayers for two additional years.

On Sept. 21, 2012, the Pipeline and Hazardous Materials Safety Administration (PHMSA) issued a second notice and request for comments in the Federal Register proposing revisions to 1) the hazardous liquid pipeline system accident report form, 2) the natural and other gas transmission and gathering pipeline systems incident report form, and 3) the annual report form for gas transmission and gathering systems.

On Dec. 23, 2011, the United States Environmental Protection Agency (EPA) proposed changes to the National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial, Commercial and Institutional Boilers and Process Heaters (the Boiler MACT) Rule.

On Friday, Sept. 20, 2013, the U.S. Environmental Protection Agency proposed rules to regulate greenhouse gas emissions from new fossil fuel-fired electric generating units.

Michigan Governor Rick Snyder signed into law within the last month a variety of bills amending the Natural Resources and Environmental Protection Act (NREPA) and other legislation reforming Michigan environmental law compliance and enforcement requirements.

EPA has added nine additional per- and polyfluoroalkyl substances (PFAS) compounds to Toxic Release Inventory (TRI) reporting requirements...

On Oct. 13, the Pipeline and Hazardous Materials Safety Administration (PHMSA) published a proposed rule governing liquid pipeline safety, 49 CFR Part 195.

Significant changes are expected for the upcoming 2010 proxy season. One certain change is the loss of broker discretionary votes in the election of directors.

Earlier this month, Assistant Attorney General Tony West of the U.S. Department of Justice (DOJ) gave a speech at the Twelfth Annual Pharmaceutical Regulatory and Compliance Congress in Washington, D.C.

FDA recently issued a draft Guidance interpreting "substantive summary" and "significant decision" as used in section 603.

Part of what the medical device industry bought with the substantial increase in FDA user fees to which it agreed in the FDA Safety and Innovation Act of 2012 was an independent review and evaluation of FDA’s primary premarket device review programs, the 510(k) and PMA programs.

The FDA recently issued a final guidance titled, "The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications."

The FDA recently issued a final Guidance document titled "Medical Devices: Pre-Submission Program and Meetings with FDA Staff" to provide advice to medical device manufacturers who want FDA’s input before submitting an IDE, HDE, 510(k), or PMA.

The FDA recently released a draft guidance titled, "Distribution of Scientific and Medical Publications on Unapproved Uses – Recommended Practices."

On October 20, 2011, the Center for Medicare and Medicaid Services (CMS) and the Department of Health and Human Services Office of Inspector General (OIG) released an Interim Final Rule (OIG Rule) providing fraud and abuse waivers for accountable care organizations (ACOs) that participate in the Medicare Shared Savings Program (Shared Savings Program).

The U.S. Court of Appeals for the Third Circuit recently issued a non-precedential opinion affirming a finding that alleged food labeling claims asserted against Johnson & Johnson were expressly preempted by the Food, Drug & Cosmetic Act.