• where experts go to learn about FDA
  • Year: 2010

    • Rep. Schakowsky Introduces Safe Cosmetics Act of 2010; Bill Would Increase Regulation of CosmeticsJuly 21st, 2010

      By Kurt R. Karst –    Earlier this week, Rep. Jan Schakowsky (D-IL), along with Reps. Ed Markey (D-MA) and Tammy Baldwin (D-WI), introduced H.R. 5786, the Safe Cosmetics Act of 2010.  The bill would significantly change the regulatory structure of cosmetics in the U.S., …

    • FDA Seeking Public Comment on Federal Menu Labeling RequirementsJuly 20th, 2010

      By Susan J. Matthees – FDA recently announced that the Agency is seeking public comments on how to implement section 4205 of the Patient Protection and Affordable Care Act of 2010 (“PPACA”), which requires certain restaurants and vending machines to disclose nutrition information.  The docket opened on …

    • Federal Circuit Denies Rehearing Petition in LEVAQUIN Patent Term Extension CaseJuly 19th, 2010

      By Kurt R. Karst –    Last week, the U.S. Court of Appeals for the Federal Circuit denied Lupin Pharmaceuticals, Inc.’s (“Lupin’s”) Petition for Rehearing en banc of a May 10, 2010 panel decision in Ortho-McNeil Pharmaceutical, Inc. v. Lupin Pharmaceuticals, Inc. in which the Court affirmed …

    • Senate FY 2011 FDA Appropriations Bill Should be Another Big Step Forward for Rare and Neglected Disease Patients and AdvocatesJuly 16th, 2010

      By Kurt R. Karst –    As the U.S. Senate Committee on Appropriations begins its markup and consideration of appropriations bills for Fiscal Year (“FY”) 2011, and in particular the Agriculture, Rural Development, FDA, and Related Agencies Appropriations bill (S. 3606), rare and neglected disease …

    • Whistleblowers: A Potential Problem for EveryoneJuly 15th, 2010

      In the May/June 2010 edition of FDLI Update, HP&M Director John R. Fleder published his latest article on enforcement matters.  This article is entitled “Whistleblowers: Treat Them With Kid Gloves.”  The article addresses various issues that companies face when they are confronted with employees who …

    • Nestle Unit’s Settlement with FTC Contains New Provisions Regarding SubstantiationJuly 15th, 2010

      By Peter M. Jaensch – On July 14, 2010, the Federal Trade Commission (“FTC”) announced an agreement with Nestle HealthCare Nutrition, Inc. (“Nestle”) to settle an FTC investigation with regard to alleged false and misleading health claims. The FTC's Complaint arose from claims made by …

    • HP&M Attorney Elected to USP Expert CommitteeJuly 14th, 2010

      Hyman, Phelps & McNamara, P.C. (“HP&M”) is pleased to announce that Diane B. McColl has been elected to  the U.S. Pharmacopeial Convention’s (“USP’s”) Expert Committee for the Food Chemicals Codex (Monographs – Food Ingredients) for the 2010-2015 cycle.  The committee develops new monographs and revises …

    • FTC Continues Focus on Cold and Weight Loss Supplement Claims, Settles with Iovate for $5.5MJuly 14th, 2010

      On July 14th, the FTC announced the settlement of a significant false advertising case against Iovate Health Sciences U.S.A. and Canadian affiliates for false weight loss, cold, flu and allergy claims relating to 5 of the company's products.   The settlement includes $5.5M for refunds to …

    • Graceway Sues FDA Over Generic ALDARA Cream Decisions; Alleges that Petition Response is Contrary to Basic Science, Common Sense, and PrecedentJuly 13th, 2010

      By Kurt R. Karst –    Although it took a little longer than we expected, late last week, Graceway Pharmaceuticals, LLC (“Graceway”) sued FDA in the U.S. District Court for the District of Columbia requesting declaratory and injunctive relief with respect to the Agency’s January 2010 denial …

    • FDA Releases Draft of Class-Wide Opioid REMSJuly 12th, 2010

      By William T. Koustas – FDA recently released a draft of it class-wide opioid REMS in preparation for an advisory committee meeting on the issue.  The Joint Meeting of the Anesthetic and Life Support Drugs Advisory Committee and the Drug Safety and Risk Management Advisory …

    • Compounding Pharmacies Strike back Against Government ActionsJuly 11th, 2010

      By John R. Fleder – It is hardly a secret that FDA’s favorite regulated industry is certainly not the businesses that compound pharmaceutical products.  For years FDA has struggled to establish an enforcement mechanism that passes muster with Congress and the courts.  Two compounding pharmacies have …

    • HHS Issues Proposed HIPAA/HITECH RuleJuly 9th, 2010

      By Jeffrey N. Wasserstein – On July 8, 2010, the Office for Civil Rights of the U.S. Department of Health and Human Services announced the issuance of its long-awaited proposed rule (in prepublication form) relating to the modification to the HIPAA Privacy, Security and Enforcement Rules under …

    • Analysis Shows Patent Use Codes Have Doubled Since August 2003July 8th, 2010

      By Kurt R. Karst – With all of the hubbub over Patent Use Codes (“PUCs”) since the U.S. Court of Appeals for the Federal Circuit issued its April 2010 decision in Novo Nordisk A/S v. Caraco Pharmaceutical Laboratories, Ltd. addressing whether the patent delisting counterclaim …

    • D.C. Circuit Affirms District Court Ruling Concerning Losartan 180-Day Exclusivity Forfeiture IssueJuly 6th, 2010

      By Kurt R. Karst –    Earlier today, a 3-judge panel (Judges Tatel, Griffith, and Kavanaugh) of the U.S. Court of Appeals for the District of Columbia Circuit issued a 2-page per curiam judgment (without memorandum) affirming the U.S. District Court for the District of …

    • Coalition for Mercury-Free Drugs Fails to Prove Standing in Thimerosal CaseJuly 5th, 2010

      By Alexander J. Varond* & Kurt R. Karst – Recently, the U.S. District Court for the District of Columbia dismissed a case brought by the Coalition for Mercury-Free Drugs (“Coalition”). Judge Reggie B. Walton ruled that the Coalition lacked standing to ask the court to ban …