Good Documentation Guideline (Chapter 1029 USP)

Good Documentation Guideline (Chapter 1029 USP)


This session will wrap up the general concept and will provide

information as to what needs to be documented in certain records.

Why should you Attend:
If you are involved in any product manufacturing, knowing GDP

regulations is a must for you. Manufacturing is prone to any kind of

errors, deviations, unforeseen events. It is of utmost importance to

know what you need to do in case of any unforeseen situations.

Areas Covered in the Session:
Laboratory records
Equipment-related documentation
Deviations and investigations
Batch records
Certificate of Analysis (C of A)*
Standard Operating Procedure (SOP)*
Protocols & reports*
Analytical procedures*
Training documentation
Retention of documents

Who Will Benefit:
Quality Assurance & Quality Control Personnel / Managers
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: compliance4all14@gmail.com

Ad Reference ID: 3195c109501559b2

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