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Jill Wechsler is Pharmaceutical Technology's Washington Editor, firstname.lastname@example.org.
The White House initiative to encourage production of essential medicines in the United States calls on FDA to set the parameters for and implement main aspects of the program.
The White House initiative to encourage production of essential medicines in the United States calls on FDA to set the parameters for and implement main aspects of the program. Under the executive order issued by President Trump on August 6, 2020, FDA first will determine which medicines fall under the program’s requirements. In addition, the agency will collect additional information from manufacturers on drug and ingredient origins and accelerate approval of qualifying products and their production facilities.
FDA has 30 days to draw up a list of “essential medicines, medical countermeasures, and their critical inputs” (i.e., APIs and other components) and another 60 days to finalize it. The list will cover therapies and medical products that the US “must have available” at all times, particularly treatments for infectious diseases and to protect against chemical, biological, radiological, and nuclear (CBRN) threats.
To ensure demand for domestically made medicines, federal agencies that purchase drugs, including the Department of Health and Human Services (HHS), the Department of Defense, and the Department of Veterans Affairs, will develop plans in 90 days for steering procurement and contracts to those essential medicines produced at home. Those agencies will have to submit annual reports in 2021 on where they source these critical products. The US Trade Representative, moreover, will exclude those listed products from free trade agreements, while federal agencies will look to revise environmental and other regulations likely to inhibit construction of new pharmaceutical facilities in the US.
There are some notable exceptions to the program. The Buy American requirements won’t apply to medicines not available in sufficient quantities in the US, to US-made products that are 25% more expensive than imports; or in cases of a national emergency. At the same time, the new policies will aim to combat trade in counterfeit goods and protect intellectual property.
FDA also will seek to reduce supply chain vulnerabilities by collecting information on the sources of and shortages in critical drugs and medical devices and their ingredients, plus information on the date of a facility’s most recent inspection and the results of such inspections. To accomplish these goals, the agency will identify where new regulations or guidance are needed to collect production information and will negotiate with other countries to increase foreign inspections—including unannounced site visits—of firms producing essential medicines. And the government will limit imports from manufacturers that refuse or unreasonably delay an inspection.
At the same time, FDA will encourage pharma manufacturers to shift production to the US by offering accelerated approval of essential medicines made in the US, particularly those needed to counter infectious disease and CBRN threat preparedness. The agency will issue guidance on developing advanced manufacturing techniques for domestic production of essential therapies, while also looking to identify and propose changes in laws and regulations found to erect barriers to domestic production efforts.
A main objection to the “Buy American” policy for pharmaceuticals is that domestically produced critical medicines are likely to be more expensive than those made overseas. Generic-drug makers, in particular, acknowledge that APIs and drugs from China and India are cheaper than those made in the US and that government contracts for pharmaceuticals need to assume higher prices for American-made products.
In this light, the initiative to increase purchases from domestic producers runs counter to an earlier White House announcement advancing four drug price control initiatives, including an international reference pricing scheme for drugs and biologics. President Trump issued executive orders on July 24 that call for certain health centers to pass on price discounts on insulin and epinephrine and to allow drug imports from Canada and other countries, policies announced previously and already undergoing analysis for impact and implementation. Another proposal would reduce rebates paid to “middlemen” managing Medicare drug plans, which analysts say would raise premiums for beneficiaries. Trump again floated the idea of setting an international pricing index, or “most favored nation” policy, to link prices paid for Medicare Part B medicines to those paid overseas.
Manufacturers were livid that the White House was proposing such massive changes in operations with the Buy American plan and a foreign pricing index at a time of great industry focus and investment in developing treatments to combat COVID-19. Big Pharma CEOs rejected Trump’s invitation to come to a White House meeting to discuss these proposals, further escalating tensions between biopharma companies and the administration. Trump has more support for his drug pricing proposals from Democrats, but no further action is expected this year.