Which are Compliant for Inspections for a [GXP Compliance]

  • 150.00 Dollar US$
  • Published date: September 12, 2018
    • Fremont, California, United States

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

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