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Good Documentation Guideline (Chapter 1029 USP)


Overview: Compliance with GDP ensures an auditable account of work. It ensures integrity and control of documents and is a key requirement for a developed quality system.

Why should you Attend:
GDP is part of GMP and if you know it by heart, it prevents a lot of wrongdoings and minimizes the chance of being spotted by the regulatory bodies in their audits.

Areas Covered in the Session:
Standard Operating Procedure (SOP)
Protocols & reports
Analytical procedures
Training documentation
Retention of documents

Who Will Benefit:
Laboratory Personnel / Managers
Validation Specialists
Clinical Trial Personnel
Project Managers

Speaker Profile:
Dr. Afsaneh Motamed Khorasani PhD is a Medical and scientific Affairs expert and a Senior Scientist with a strong background in biomedical science and clinical trial/research. She has a tenured and diverse range of experience in medical affairs, basic and industrial clinical research and development, clinical trials, Medical and regulatory writing and intellectual property.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

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