Search for: "Hyman, Phelps & McNamara, P.C." Results 81 - 100 of 150
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13 Nov 2023, 3:15 am by Hyman Phelps McNamara
 Program highlights include: Spotlight on FDA’s Newly Proposed ACNU Rule Updates on Monograph Reform Implementation Advertising, Labeling and Claims Substantiation Essentials Exploring the Recent Wave of Rx-OTC Drug Switches Hyman, Phelps & McNamara, P.C. [read post]
14 Apr 2022, 10:49 am by Hyman Phelps McNamara
  Over the course of two days, this event will provide impactful and practical programming all geared towards assessing the implications and imprimaturs of court cases, legislation, and industry behaviors which affect the patent endgame and the pursuit of related profits. 2022 agenda highlights include: The Viability of Written Description as a Compelling Invalidity Defense Clarity On What Satisfies Section 1400(b)’s Venue Requirements in the Hatch-Waxman Context Whether a Skinny Label… [read post]
29 Jan 2023, 6:09 pm by Kurt R. Karst
The analysis was prepared for Pharma Conference’s conference on February 8 and 9 in San Diego (“Current Hot GMP Topics”), linked here, where Hyman, Phelps & McNamara, P.C., Director Doug Farquhar will be presenting on three areas: enforcement areas of primary concern, the conduct of internal investigations, and contacting FDA about inspections. [read post]
5 Feb 2012, 3:08 pm by FDABlog HPM
  Among other notable provisions, the proposed regulation would: Require states to convert to an actual acquisition cost basis for Medicaid prescription drug payment  Expand the MDRP to the U.S. territories Apply a statutory alternative rebate for line extensions of oral solid dosage form innovator drugs, not only to new formulations, but new indications, combination products, and products marketed by companies independent of the company marketing the original drug Limit wholesaler sales… [read post]
12 Apr 2023, 5:43 pm by Hyman Phelps McNamara
On Thursday, April 20, from 1:30-3:00pm, John Claud of Hyman, Phelps & McNamara, P.C. will present a webinar entitled “Medical Device Enforcement: Latest Developments from the FDA, DOJ and FTC. [read post]
8 Oct 2007, 9:58 pm
Hyman, Phelps &;amp; McNamara, P.C. submitted a letter on behalf of an unnamed company that has a tentatively approved ANDA for ramipril capsules. [read post]
9 Nov 2022, 3:39 pm by Hyman Phelps McNamara
As we have done in the past for the initial and each quinquennial reauthorization of the drug and medical device user fee laws—in 1992, 1997, 2002, 2007, 2012, and 2017—Hyman, Phelps & McNamara, P.C. has prepared a detailed Summary and Analysis of FUFRA. [read post]