This Event has Passed
Monday, November 12, 2018
10:00 AM - 11:00 AM
10:00 AM - 11:00 AM See all dates and Times
https://www.compliance4all.com/control/w_product/~product_id=502185LIVE?channel=upcomingevents_Nov_2018_SEO
Overview: This webinar will help Sponsors, CROs in the US, EU and internationally,understand how to write SOPs to comply with inspection requirements.
Why should you Attend:
This webinar will assist you to prepare for inspection of SOPs, particularly since such inspection readiness of SOPs are taking considerable time to prepare for. Inspections of SOPs of critical activities that impact business success on several levels. Therefore, preparation and management of the inspection and audit process of SOPs is an important business activity, not just a distraction from day to day routine.
Areas Covered in the Session:
Understand why we need written SOP procedures
Gain an insight into expectations for an effective written documentation
Understand Regulatory requirements for the creation, compliance and maintenance of SOPs
Gain techniques for creating effective SOPs and other written documents to minimize costly revisions
Who Will Benefit:
Clinical Research Associates
Clinical Research Archiving and Document Management Personnel
Quality Assurance Managers and Auditors
Clinical Development Managers and Personnel
Manufacturing
Pharmacovigilance
Laboratories
Speaker Profile:
Dr. Laura Brown , PhD, MBA, Diploma Clinical Sciences, is an independent QA and training consultant in the pharmaceutical industry. She is a managing director with LB Training and Development Ltd., course director for the M.Sc. in Clinical Research, School of Pharmacy at the University of Cardiff, and course director for M.Sc.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
Why should you Attend:
This webinar will assist you to prepare for inspection of SOPs, particularly since such inspection readiness of SOPs are taking considerable time to prepare for. Inspections of SOPs of critical activities that impact business success on several levels. Therefore, preparation and management of the inspection and audit process of SOPs is an important business activity, not just a distraction from day to day routine.
Areas Covered in the Session:
Understand why we need written SOP procedures
Gain an insight into expectations for an effective written documentation
Understand Regulatory requirements for the creation, compliance and maintenance of SOPs
Gain techniques for creating effective SOPs and other written documents to minimize costly revisions
Who Will Benefit:
Clinical Research Associates
Clinical Research Archiving and Document Management Personnel
Quality Assurance Managers and Auditors
Clinical Development Managers and Personnel
Manufacturing
Pharmacovigilance
Laboratories
Speaker Profile:
Dr. Laura Brown , PhD, MBA, Diploma Clinical Sciences, is an independent QA and training consultant in the pharmaceutical industry. She is a managing director with LB Training and Development Ltd., course director for the M.Sc. in Clinical Research, School of Pharmacy at the University of Cardiff, and course director for M.Sc.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
