Food and Drug Administration Safety and Innovation Act
The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012. It gives the United States Food and Drug Administration (FDA) the authority to collect user fees from the medical industry to fund reviews of innovator drugs, medical devices, generic drugs and biosimilar biologics. It also reauthorizes two programs that encourage pediatric drug development.
Synthetic drug abuse prevention
The law also contains the Synthetic Drug Abuse Prevention Act of 2012. The legislation bans synthetic compounds commonly found in synthetic marijuana ("K2"[1] or "Spice"), synthetic stimulants ("bath salts"[2]), and hallucinogens, by placing them under Schedule I of the Controlled Substances Act.
Generating antibiotic incentives now
Under "Title VIII — Generating antibiotic incentives now" (GAIN), sections 801, 802, 803 provide designated candidate antibiotics ("qualifying infectious disease products" or QIDPs) extension of exclusivity, priority review, and fast track approval.
Breakthrough therapy
Section 902 of the Act provides for a new designation - Breakthrough Therapy Designation for drugs that may be significantly better treatments for serious diseases or conditions.[3] On November 13, 2013 the FDA approved obinutuzumab (trade name Gazyva) by Hoffmann-La Roche[4] for chronic lymphocytic leukemia making it the first drug to receive the coveted breakthrough therapy designation.[5][6]:358
Other
Section 618 of the FDASIA directed the Secretary of Health and Human Services, acting through the Commissioner of the United States Food and Drug Administration, and in consultation with the Office of the National Coordinator for Health Information Technology and the Chairman of the Federal Communications Commission (FCC), to develop a report that contains a proposed strategy and recommendations on an appropriate, risk-based regulatory framework for health IT, including medical mobile applications, that promotes innovation, protects patient safety, and avoids regulatory duplication. The Health IT Policy Committee formed a FDASIA workgroup and issued recommendations to ONC, FDA, and FCC as of the September 4th, 2013 HIT Policy Committee meeting.[7]
References
- ↑ Vashi, Sonam (September 26, 2012). K2 Trend Not Slowing Down WebMD Medical News via KOKI-TV
- ↑ Marder, Jenny (September 20, 2012). Bath Salts: The Drug That Never Lets Go. PBS NewsHour
- ↑ "Significant Amendments to the FDC Act", FDASIA
- ↑ "Final Recommendation for Obinutuzumab (Gazyva) for CLL Pan-Canadian Oncology Drug Review (pERC) Meeting: December 18, 2014; Early Conversion: pCODR" (PDF). Pan-Canadian Oncology Drug Review via Canadian Agency for Drugs and Technologies in Health. 27 January 2015. Retrieved 22 November 2015.
- ↑ FDA approves Gazyva for chronic lymphocytic leukemia: Drug is first with breakthrough therapy designation to receive FDA approval, FDA News Release, FDA, November 13, 2013, retrieved July 20, 2015
- ↑ Kakkar, A.; Balakrishnan, S. (October 2015). "Obinutuzumab for chronic lymphocytic leukemia: promise of the first treatment approved with breakthrough therapy designation". Journal Of Oncology Pharmacy Practice (Ipswich, MA) 21 (5): 358–363. doi:10.1177/1078155214534868. ISSN 1078-1552. Retrieved 23 November 2015. via EBSCO
- ↑ http://healthit.gov/policy-researchers-implementers/health-it-legislation
External links
- Regulatory Information: Food and Drug Administration Safety and Innovation Act
- Full Text of the Synthetic Drug Abuse Prevention Act of 2012
- FDA Expedited programs guidance e.g. Fast track, breakthrough therapy, accelerated approval, priority review.