This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful strategies for medical devices, including definitions and classifications, elements of regulatory strategy, sources of regulatory intelligence, selection of development and product clearance/approval pathways.
Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900902SEMINAR?allconferencealerts_SEO
This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful strategies for medical devices, including definitions and classifications, elements of regulatory strategy, sources of regulatory intelligence, selection of development and product clearance/approval pathways.
Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900902SEMINAR?allconferencealerts_SEO
This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful strategies for medical devices, including definitions and classifications, elements of regulatory strategy, sources of regulatory intelligence, selection of development and product clearance/approval pathways.
Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900902SEMINAR?allconferencealerts_SEO will be held in Boston, ma,United States on date 2017-06-23
Deadline for abstracts/proposals : 21st June 2017
Organized By :NetZealous DBA as GlobalCompliancePanel
Keynote Speakers : Dr. Thomas E. Colonna earned a bachelor of science in microbiology from the University of Sciences in Philadelphia (formerly the Philadelphia College of Pharmacy and Science), a Ph.D. in molecular biology from the Johns Hopkins University, and a law degree from the Georgetown
Conference Highlights :Regulatory professionals working in the medical device field