Good Documentation Practices (GDP) 2016

Topics

• Documentation System
• What is Documentation
• Good Documentation Practices
• Types of Documents
• Documentation Processing and Control
• Good Documentation Requirements
• Guidance Documents for GDP

Who should Attend

• 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