Good Documentation Guideline (Chapter 1029 USP)
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Category Good Documentation Guideline, 1029 USP, USP Online, laboratories and clinical trials, Standard Operating Procedure, good documentation practices, what is sop means, standard operating procedure examples
Deadline: February 06, 2019 | Date: February 07, 2019
Venue/Country: Online, U.S.A
Updated: 2018-12-07 14:56:45 (GMT+9)
Call For Papers - CFP
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 recordsEquipment-related documentationDeviations and investigationsBatch recordsCertificate of Analysis (C of A)*Standard Operating Procedure (SOP)*Protocols & reports*Analytical procedures*Training documentationRetention of documentsWho Will Benefit:Quality Assurance & Quality Control Personnel / ManagersLaboratory Personnel / ManagersValidation SpecialistsClinical Trial PersonnelProject ManagersSpeaker 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 $150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
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