Good Documentation Practice for GxP Environments 2016 is a webinar that covers topics such as:
- Why document?
- FDA 101: who is the FDA, regulations, guidances, documentation and industry
- What documentation does FDA look for during an inspection?
- What needs to be documented?
- Examples and exercises for good documentation
- What do the GMP, GCP, and GLP regulations and guidances say about documentation?
- Summary/ Q&A
Good Documentation Practice for GxP Environments 2016 is intended for attendees from:
- R&D
- GxP personnel involved with GxP Documentation
- Quality
- Production
- Regulatory
