DUBLIN--(BUSINESS WIRE)--Research and Markets (http://www.researchandmarkets.com/research/zz3g74/fda_drug_approval) has announced the addition of the "FDA Drug Approval Process (10-11 September 2015 - London, UK)" conference to their offering.
This seminar, by a US lawyer with over 40 years of experience dealing with pharmaceutical regulation in the United States and Europe, will provide a general introduction to all aspects of the US drug approval process. It will also cover the organisation and structure of the Food and Drug Administration, recent amendments to the FDA's procedures designed to expedite the testing and approval of new medicines and other topics of current interest.
Why You Should Attend:
- Structure and functions of the FDA
- Historical background
- General regulatory requirements
- Regulation of preclinical and clinical research
- New drug application process
- Biologics (including biosimilars)
- Generic drugs
- OTC drugs
- Special issues
For more information visit http://www.researchandmarkets.com/research/zz3g74/fda_drug_approval
