Developing and Maintaining Pre-marketing Master Regulatory Files 2012
09 Oct 2012
Webinar
Key Topics
GXP requirements
Regulatory master files
TMF, DMF
Regulatory chronology
Quality audits
Organization
Good documentation practices
The Developing and Maintaining Pre-marketing Master Regulatory Files 2012 is recommended for:
Quality assurance/control
Regulatory affairs personnel
Project managers
Clinical operations
Clinical Trial Associates (CTA)
Clinical Research Associates (CRA)
Pharmacovigilance specialists
Medical monitors
Contract manufactures
Site managers
Past Events
Developing and Maintaining Pre-marketing Master Regulatory Files 2012 - 09 Oct 2012, Webinar (32888)
Developing and Maintaining Pre-marketing Master Regulatory Files - Webinar By GlobalCompliancePanel 2012 - 01 Aug 2012, Webinar (31866)
Developing and Maintaining Pre-marketing Master Regulatory Files 2026
Important
Please, check "Developing and Maintaining Pre-marketing Master Regulatory Files" official website for possible changes, before making any traveling arrangements
