Good Documentation Practices (GDP) 2016 is a webinar that covers topics such as:
- Documentation System
- What is Documentation
- Good Documentation Practices
- Types of Documents
- Documentation Processing and Control
- Good Documentation Requirements
- Guidance Documents for GDP
Good Documentation Practices (GDP) 2016 is intended for:
- Clinical research associates
- Anyone who authors, reviews, and audits documents and records in FDA-regulated pharmaceutical, biotechnology, and medical device industries
- Laboratory personnel
- Manufacturing/production personnel
- Document control associates
- Research and development associates
- QA/QC specialists
- Batch record reviewers
- Quality assurance auditors
- Validation engineers
- Regulatory compliance associates and managers
