The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: February 7, 2019 from 10am to 11am
Street: 161 Mission Falls Lane, Suite 216,
Website or Map: https://www.compliance4all.co…
Phone: Event Manager
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Dec 11, 2018
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:
Deviations and investigations
Certificate of Analysis (C of A)*
Standard Operating Procedure (SOP)*
Protocols & reports*
Retention of documents
Who Will Benefit:
Quality Assurance & Quality Control Personnel / Managers
Laboratory Personnel / Managers
Clinical Trial Personnel
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
Compliance4All DBA NetZealous,