Biologic product identification and US pharmacovigilance in the biosimilars era

Author:

Felix Thomas,Johansson Torbjörn T,Colliatie Jodi A,Goldberg Michael R,Fox Andrew R

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Reference11 articles.

1. IMS Health. Shaping the Biosimilars Opportunity: A Global Perspective on the Evolving Biosimilars Landscape. http://www.imshealth.com/ims/Global/Content/Home%20Page%20Content/IMS%20News/Biosimilars_Whitepaper.pdf (IMS Health, London, 2011; accessed January 17, 2014).

2. Biologics Price Competition and Innovation Act of 2009. http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/UCM216146.pdf (accessed 21 October 2013).

3. US Food and Drug Administration. Guidance for Industry: Scientific Considerations in Demonstrating Biosimilarity to a Reference Product (FDA; Rockville, MD, 2012).

4. Government Accountability Office. Food and Drug Administration Response to Heparin Contamination Helped Protect Public Health; Controls That Were Needed for Working with External Entities Were Recently Added (GAO; Washington, DC, 2010).

5. Olson, K. Alliance for Safe Biologic Medicine—Prescriber Survey. http://safebiologics.org/resources/wp-content/uploads/2012/09/ASBM-Survey-2.pdf (ISR, 2012; accessed 21 October 2013).

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