Good Documentation Guideline (Chapter 1029 USP)

Overview:
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