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2018 - Good Documentation Guideline (Chapter 1029 USP)



VenueFremont, USA - United States USA - United States

KeywordsClinical Trial Personnel; Validation Specialists; Quality Assurance


Topics/Call fo Papers

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
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407

Last modified: 2018-08-10 14:32:25