Good Documentation Guideline (Chapter 1029 USP)

Date : 7th February 2019 to 7th February 2019

Place : United States, Fremont

Website :https://www.compliance4all.com/control/w_product/~product_id=502295LIVE?channel=copybook_Feb_2019_SEO

Contact Person:Event Manager

Description:

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: [email protected]

Good Documentation Guideline (Chapter 1029 USP) will be held in Fremont,United States on date 2019-02-07

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Deadline for abstracts/proposals : 5th February 2019

Keynote Speakers :

Venue :Fremont, CA, USA

Check the event website for more details.