Record Keeping Best Practices [FDA and EMA] Documentation

Overview:Good documentation Practices (GDP) is an essential factor that needs to be closely followed by the personnel in any regulated environment as a process for a successful project completion including observations of unanticipated responses that are required to be accurately recorded and verified.
Why should you Attend:If you are involved in any product manufacturing, knowing GDP regulations is a must for you. It prevents a lot of errors and minimizes the chance of being spotted by the regulatory bodies in their audits.
Areas Covered in the Session:Definition, Purpose, and ImportanceGeneral Rules and Principles of GDPRequirements of RecordsGeneral Tips in GDPSignature / initial and the meaningCopying recordsDocument maintenance
Who Will Benefit:Laboratory Personnel / ManagersValidation SpecialistsClinical Trial PersonnelProject 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: +1-800-447-9407Email: support@compliance4All.com