Food and Drug Administration Amendments Act of 2007

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name= Food and Drug Administration Amendments Act of 2007
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acronym= FDAAA
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amendments=On September 27, 2007, President George W. Bush signed the ‘‘‘Food and Drug Administration Amendments Act of 2007’’’ into law. This new law is an important step for the Food and Drug Administration (FDA). It reviewed, expanded, and reaffirmed several existing pieces of legislation regulating the FDA. These changes will allow the FDA access to much-needed resources that will enable the agency to better protect American consumers by allowing more comprehensive reviews of potential new drugs and devices. [ [http://www.fda.gov/oc/initiatives/advance/fdaaa.html Law Strengthens FDA ] ]

Prescription Drug User Fee Act (PDUFA) (IV)

The Prescription Drug User Fee Act was first enacted in 1992 to allow the FDA to collect “user fees” from biotechnology and pharmaceutical companies. Since then, it has been reauthorized three times; first in 1997, then 2002, and most recently with the passage of the FDAAA in 2007. The purpose of these fees is to provide resources to the FDA that help them more effectively review potential new drugs. [ [http://www.bio.org/healthcare/pdufa/ BIO | The Prescription Drug User Fee Act (PDUFA) ] ] The most recent reauthorization will further expand on the previous policy. It aims to broaden and upgrade the drug safety program, allocate more resources for television advertising, and theoretically allow the FDA to more efficiently review and approve safe and effective new drugs for consumers. [ [http://www.fda.gov/oc/pdufa/ Prescription Drug User Fees ] ] Since the original inception of the act, skeptics have raised concerns that this act means that the FDA is partially funded by the industry it regulates.

Medical Device User Fee and Modernization Act (MDUFMA)

•Allows for user fees which will allow the FDA to make significant improvements in the medical device review program.

•Establishment inspections may be conducted by accredited persons (third-parties), and establish new regulatory requirements for reprocessed single-use devices. FDAAA changes the medical device establishment registration requirements. Although both foreign and domestic drug manufacturers still must register establishments

Best Pharmaceuticals for Children Act (BPCA) - encourages more studies in children and promotes the development of treatments for children.

•Intended to improve FDA and applicant accountability for the agreed-upon pediatric studies.

•FDAAA broadens the definition of “pediatric studies” to include preclinical studies, and narrows the timeframe for sponsors to qualify for pediatric exclusivity.

Pediatric Research Equity Act (PREA) – continues FDA's authority to require studies in children concerning certain medical products and under other specific circumstances.

Reagan-Udall foundation - to modernize product development, accelerate innovation, and enhance product food safety with clinical trial registries provisions by an advisory committee intended to enhance drug safety.

•Also created to “modernize medical, veterinary, food, food ingredient, and cosmetic product development, accelerate innovation, and enhance product safety.”

Advisory Committee Conflicts Of Interest - continues the requirement that all individuals under consideration for appointment to serve on an FDA advisory committee disclose to the Agency all financial interests that would be affected by the committee’s actions.

References

External links

* http://www.fda.gov/oc/initiatives/advance/fdaaa.html
* http://www.fda.gov/oc/initiatives/HR3580.pdf