The Developing and Maintaining Pre-marketing Master Regulatory Files 2012 is a webinar that covers topics such as:
- 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
