How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit 2011
19 Aug 2011
Webinar
This webinar is focused on How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit 2011.
This webinar on How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit 2011, brings together Clinical Research Scientists, investigators involved in the legal, regulatory and ethical issues in pharmaceutical product (Drug or device) research, Clinical Research Associates (CRAs), Safety Nurses, Clinical Research Data managers and QA / QC auditors.
Past Events
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit 2011 - 19 Aug 2011, Webinar (17434)
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit 2026
Important
Please, check "How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Pharma
