Two House members have established a group that they hope will produce legislation that leads to increased use of generic and biosimilar drugs and lower healthcare costs.
US caucus to promote generics and biosimilars
Home/Policies & Legislation
|
Posted 27/05/2011
0
Post your comment

Representatives Ms Jo Ann Emerson and Mr Peter Welch, founded the Congressional Affordable Medicines Caucus on 12 May 2011 and plan to push for an expansion of FDA’s Office of Generic Drugs, as well as trying to reduce the growth in healthcare spending.
Hopefully this lobbying by House representatives will prevent or reduce the size of cuts to the Office of Generic Drugs budget announced by US Congress, which the Generic Pharmaceutical Association (GPhA) had stated ‘would further slow generic approvals at the very time we need more, not fewer affordable medicines on the market’.
The GPhA has expressed its support of the goals of the caucus to increase the use of generic drugs and increase funding for the FDA’s Office of Generic Drugs. The GPhA feels that the US medical insurance programs Medicare and Medicaid are currently failing to take advantage of the enormous savings offered by generic drugs.
It has been estimated that an increase in generic use by even as little as a 2% by Medicaid would save the program more than US$1.3 billion. A 5% increase could save nearly US$3.3 billion.
Meanwhile, there is a massive backlog at the FDA, with more than 2,000 generic drug applications awaiting action. Since as many as 365 of those applications are related to first-time generic drugs it is no wonder the Office of Generic Drugs needs extra funding to clear this backlog. Whether this funding comes from Congress or from the much-discussed generic user fees or both–it can only be good news for the generics industry.
Related articles
Still no word from FDA on generic user fees
Negotiations on generic drug user fees
FDA user fees for assessing generic drugs
Source: GPhA
Guidelines
Canada poised to remove requirement for Phase III trials for biosimilars
European position paper on AI in medicinal product lifecycle
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
US EO: delivering Most-Favored-Nation Prescription Drug Pricing to American patients
Uruguay to establish independent AUVISA drug agency for healthcare reform
Malaysia announces Screening Package for new drugs and biologicals
Trump’s ‘One Big Beautiful Bill’: implications for US health care
US EO: delivering Most-Favored-Nation Prescription Drug Pricing to American patients

Home/Policies & Legislation Posted 03/10/2025
Uruguay to establish independent AUVISA drug agency for healthcare reform

Home/Policies & Legislation Posted 17/09/2025
Malaysia announces Screening Package for new drugs and biologicals

Home/Policies & Legislation Posted 25/08/2025
Trump’s ‘One Big Beautiful Bill’: implications for US health care

Home/Policies & Legislation Posted 14/08/2025
The best selling biotechnology drugs of 2008: the next biosimilars targets

Post your comment