Record Keeping Best Practices [FDA and EMA] Documentation

MessageThis Webinar is over
Date Nov 9, 2018
Time 10:00 AM to 11:00 AM
Cost 150.00
Online
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 Importance
General Rules and Principles of GDP
Requirements of Records
General Tips in GDP
Signature / initial and the meaning
Copying records
Document maintenance

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: support@compliance4All.com

 


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