CAE. “It is also a great resource for those who may be preparing for the EU Regulatory Affairs Certification (RAC) exam.”
Several new chapters have been added to this edition, dealing with issues of growing importance to EU regulatory professionals, including reimbursement and the health technology assessments that frequently are the basis for reimbursement decisions. There also is a new chapter on crisis management and one on the special requirements for vaccines. In light of new legislation coming into effect in 2012, there also is a new chapter devoted to pharmacovigilance.
This edition of EU Fundamentals is organized into four sections covering general information, medical devices, medicinal products and other product classifications, respectively...Regulatory Affairs Certification (RAC), the only post-academic professional credential to recognize regulatory excellence. For the original version on PRWeb visit: http://www.prweb.com/releases/prwebRegulatory-Affairs/EU-Fundamentals/prweb9763194.htm