By Aine Cryts
Amid an ongoing outcry
against rising drug costs, the Trump administration recently introduced two
importation pathways to reduce what U.S. residents pay for drugs.
Under the Safe
Importation Action Plan, the first pathway would allow states, wholesalers and
pharmacists to propose to HHS demonstration projects for importing certain
drugs from Canada. Under the second pathway, drug manufacturers could import
non-U.S. countries' versions of their drugs into the United States.
What do health plan
executives need to worry about with these two pathways? Not much, at least not
in the next couple of years, according to Jigar Thakkar, Pharm.D., a managing
director at FTI Consulting.
"There are so many
hurdles that this isn’t something that's going to happen tomorrow or in the
next year or two," Thakkar says. The hurdles include passage of
legislation to allow biologics such as insulin to be imported and the ability
of drugs imported from other countries to be tracked via FDA-TRACK, the FDA's
agency-wide performance system that monitors drugs during their journey from
manufacturer to distributors to pharmacies.
Another significant
hurdle is pushback from interest groups in Canada. Bloomberg News reported that
the Canadian Medical Association and 14 other groups sent a letter to Canada
Health Minister Ginette Petitpas Taylor protesting the Trump administration's
moves.
Deb Devereaux, senior
vice president of pharmacy at Gorman Health Group, isn't optimistic about the
success of the first pathway where drugs would be imported to the United States
from Canada. "The bottom line is the Canadian drug supply would be
exhausted in 16 months with all the U.S. states trying to avail themselves of
Canadian drugs," she says.
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