3 industry orgs suing HHS, FDA over Canadian drug imports

The Pharmaceutical Research and Manufacturers of America (PhRMA) is combining forces with two other groups to challenge the FDA final rule allowing broad, state-by-state importation of drugs from Canada.

The rule, issued in September, followed a directive from the Trump Administration to widen consumer access to lower drug prices.

The litigation cites “significant safety risks” as arising from the cross-border passage of drugs “without drug manufacturers’ authorization or oversight.”

PhRMA is joined at the plaintiff’s table by the Partnership for Safe Medicines and the Council for Affordable Health Coverage.

FDA’s co-defendants are HHS and Stephen Hahn, the FDA’s commissioner.

In announcing the action, PhRMA’s general counsel, James Stansel, states:

“It is alarming that the administration chose to pursue a policy that threatens public health at the same time that we are fighting a global pandemic. … [T]he administration is willing to divert precious FDA resources away from these efforts and to expose Americans to the risks that come with drug importation schemes.”

Along with the announcement, the groups have posted the 70-page complaint.

Dave Pearson

Dave P. has worked in journalism, marketing and public relations for more than 30 years, frequently concentrating on hospitals, healthcare technology and Catholic communications. He has also specialized in fundraising communications, ghostwriting for CEOs of local, national and global charities, nonprofits and foundations.

Around the web

The tirzepatide shortage that first began in 2022 has been resolved. Drug companies distributing compounded versions of the popular drug now have two to three more months to distribute their remaining supply.

The 24 members of the House Task Force on AI—12 reps from each party—have posted a 253-page report detailing their bipartisan vision for encouraging innovation while minimizing risks. 

Merck sent Hansoh Pharma, a Chinese biopharmaceutical company, an upfront payment of $112 million to license a new investigational GLP-1 receptor agonist. There could be many more payments to come if certain milestones are met.