Julie Tersigni

PhRMA Seeks to Eliminate Pharma Antitrust Reporting Requirements

Posted on February 18th, by and in Products Liability. No Comments

Background.

On February 7, 2014, the Pharmaceutical Research and Manufacturers of America (PhRMA), an industry group composed of research-focused pharmaceutical and biotechnology companies, filed a motion in the U.S. District Court for the District of Columbia to invalidate the Premerger Notification; Reporting and Waiting Period Requirements Final Rule (Rule) promulgated by the Federal Trade Commission.

As we discussed on December 16, 2013, this new Rule adopts an “all commercially significant rights” test to determine whether a transfer of assets has occurred in an exclusive patent license agreement.  The new Rule applies only to the pharmaceutical industry.

PhRMA’s Complaint.

PhRMA filed a Complaint seeking injunctive relief against the FTC, No. 1:13-cv-01974-BAH, (D. D.C. 2013), just days before the final rule took effect on December 16, 2013.  The Complaint alleges the following: (1) the new Rule exceeds the FTC’s statutory authority under the Hart Scott Rodino (HSR) Act; (2) … Read More »


Julie Tersigni

FTC Amendments to Premerger Notification Rules: The Who, What & Why

Posted on December 16th, by and in Products Liability. No Comments

On November 6, 2013, the Federal Trade Commission released final amendments to the Hart-Scott-Rodino Premerger Notification Rules to clarify when a transaction involving the transfer of rights to all or part of a pharmaceutical (including biologics) patent is reportable under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 (the “HSR Act”).

The final rule, which is the same as the proposed rule circulated a year ago for public comment, codifies an “all commercially significant rights” test to determine whether a transfer of rights has occurred in an exclusive patent license agreement.  Under that rule, if a patent licensor transfers all commercially significant rights to the patent, the transaction may be reportable.  The final rule states that if “limited manufacturing rights” are retained by the licensor, then the transaction may also be reportable under the Act.

The final rule, which takes effect on December 16, 2013, is available … Read More »




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PhRMA Seeks to Eliminate Pharma Antitrust Reporting Requirements

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