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Which are Compliant for Inspections for a [GXP Compliance]


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Who should attend?

Manufacturing Pharmacovigilance Laboratories CROs Project Management

Details

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: support@compliance4All.com

Prices

One Dial-in One Attendee Price: $150.00

Contact

Event Manager
support@compliance4all.com

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