Mondaq USA: Food, Drugs, Healthcare, Life Sciences > Food and Drugs Law
Arnold & Porter Kaye Scholer LLP
Following the implementation of the new EudraVigilance system, reported in our previous post, and in an attempt to streamline the monitoring of safety signals in EudraVigilance, the EMA has recently announced that ...
Reed Smith
Jurisdiction is hardly the spiciest of topics we discuss on this blog and yet it definitely qualifies for frequent-blogging status.
Wilson Elser Moskowitz Edelman & Dicker LLP
Recent developments in three New England states indicate that popular support for legalized marijuana is growing, even as the federal government reverses the hands-off policy of the previous administration.
Holland & Knight
On Jan. 4, 2018, the HHS Office of Inspector General (OIG) issued an open letter containing guidance regarding the provision of certain free drugs to federal healthcare program beneficiaries.
Mintz, Levin, Cohn, Ferris, Glovsky and Popeo, P.C.
I previously said that the year 2014 may be a game-changer for the 340B Drug Discount Program. Increasing HRSA audits, a lawsuit over the 340B Orphan Drug Rule, and HRSA's promise to issue...
Seyfarth Shaw LLP
In a recent article, senior officials with the Department of Justice's Office of the United States Trustee (the "UST"), the federal government's watchdog of the bankruptcy system ...
Troutman Sanders LLP
A case currently pending before the U.S. Court of Appeals for the D.C. Circuit challenges the applicability of the federal Contraband Cigarette Trafficking Act ("CCTA") to tribal entities.
Troutman Sanders LLP
Pending before the Mississippi Legislature is House Bill 906, which, if enacted, would increase the "tobacco equity tax" applicable to cigarettes manufactured by non-signatories ...
Archer & Greiner P.C.
The U.S. Department of Justice decision to rescind Obama-era guidance on marijuana enforcement elicited furious statements from lawmakers on both sides of the aisle.
Morrison & Foerster LLP
In December, the U.S. Food and Drug Administration (FDA) issued guidance on Technical Considerations for Additive Manufactured Medical Devices.
Jones Day
Public Meeting of FDA, USDA, and DHHS to provide information and receive public comments on agenda items and draft U.S. positions to be discussed at the 50th Session of the Codex Committee ...
Jones Day
In the November 30, 2017, Federal Register, USDA's FNS issued an interim final rule extending through school year 2018-2019 three menu-planning flexibilities ...
Jones Day
In the December 11, 2017, Federal Register, USDA's AMS announced a public hearing that was finally held on December 14, 2017, to consider a proposal ...
Jones Day
In the December 11, 2017, Federal Register, USDA's AMS adopted a final rule to amend the definition of "judge" in the rules of practice and procedure to formulate ...
Jones Day
In the January 4, 2018, Federal Register, USDA announced its withdrawal of certain advance notice of proposed rulemakings and proposed rules that were either published in the Federal Register ...
Jones Day
In the November 7, 2017, Federal Register, FDA amended the color additive regulations to provide for the safe use of calcium carbonate to color hard ...
Jones Day
In the November 13, 2017, and January 2, 2018, Federal Register, FDA amended the food additive regulations for food additives permitted ...
Jones Day
In the November 16, 2017, Federal Register, FDA announced the availability of a draft guidance for industry titled "Best Practices for Convening a GRAS Panel."
Jones Day
In the December 13, 2017, Federal Register, FDA announced the termination of the Food Advisory Committee, established on March 6, 1992.
Jones Day
On November 21, 2017, FDA announced the availability of a guidance for industry titled "Sanitary Transportation of Human and Animal Food: What You Need to Know About the FDA Regulation—Small Entity Compliance Guide."
Latest Video
Most Popular Recent Articles
Ropes & Gray LLP
The FDA also announced a Jan. 30, 2018, public workshop on the progress of the Software Precertification Pilot Program.
Archer & Greiner P.C.
New Jersey's economic recovery from the Great Recession has been among the slowest in the nation.
Wolf, Greenfield & Sacks, P.C.
Prodrugs are inactive compounds designed to be converted into pharmaceutically active metabolites following delivery to a patient.
Reed Smith
Friday December 8 was a day with two items that are particularly noteworthy because of their potentially momentous implications.
Reed Smith
Having already issued our posts on the best and worst cases of 2017, we will resist the temptation to comment on the year as a whole, particularly on the powder keg that is politics.
Morrison & Foerster LLP
"Make fine lines and wrinkles disappear!" "Reduce the visibility of fine lines and wrinkles!"
McLane Middleton, Professional Association
Although New Hampshire has long been cited as a state with significant alcoholism issues, the sheer magnitude and scope of the opioid crisis has businesses reeling on a number of fronts.
Thompson Coburn LLP
Homeopathic medicine has long occupied a niche in American culture. Since 1988, with the issuance of the Compliance Policy Guide, § 400.400, ...
McDermott Will & Emery
While continuing appropriations acts did not remove this provision, the Trump Administration's stance on regarding marijuana was made clear.
Reed Smith
FDA broadly defines CDS software to include any software function that meets the first three criteria.
Article Search Using Filters
Related Topics
Mondaq Advice Center (MACs)
Popular Authors
Popular Contributors
Up-coming Events Search
Tools
Font Size:
Translation
Channels
Mondaq on Twitter
Partners
In association with