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Good Documentation Practices (GDP) 2016
07 Jul 2016
Webinar
Home
Good Documentation Practices (GDP) 2016
Key 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
Read more
Past Events
Good Documentation Practices (GDP) 2016 - 07 Jul 2016, Webinar
(52566)
Good Documentation Practices (GDP) 2026
Important
Please, check "Good Documentation Practices (GDP)" official website for possible changes, before making any traveling arrangements
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Health & Medicine:
Medical device
Science:
Life Sciences & Biology
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