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
Retention of documents
Who Will Benefit:
Laboratory Personnel / Managers
Clinical Trial Personnel
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
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