How to Write SOPs which are Compliant for Inspections for a GXP Compliance 2018

  • 12 Nov 2018
  • Webinar

Description

How to Write SOPs which are Compliant for Inspections for a GXP Compliance 2018 is a webinar that covers topics such as:

  • Expectations for an effective written documentation
  • Why we need written SOP procedures
  • Creating effective SOPs and other written documents to minimize costly revisions
  • Regulatory requirements for the creation, compliance and maintenance of SOPs
  • How training and implementation of SOPs should be carried out to meet inspectors expectations
  • Roles and responsibilities for the review and approval of written documents consistent with compliance requirements
  • Effective control, archival and disposal of SOPs

How to Write SOPs which are Compliant for Inspections for a GXP Compliance 2018 is intended for:

  • Clinical Research Associates
  • Drug Research and Development Managers and Personnel
  • Quality Assurance Managers and Auditors
  • Clinical Research Archiving and Document Management Personnel
  • Manufacturing
  • Clinical Development Managers and Personnel
  • Laboratories
  • Pharmacovigilance
  • Project Management
  • CROs
  • Sponsors who Have their Own Laboratories for Analyzing Clinical Trial Samples
  • Sponsors and Non-Commercial Sponsors
  • Laboratories Analyzing Samples from Clinical Trials
  • Consultants
  • Clinical Trial Supply
  • Regulatory Affairs
  • To those Departments who have SOPs
  • Document Management
  • Legal, Regulatory Authorities and all Other Professionals who want to know More about Inspection of SOPs

Past Events

Important

Please, check "How to Write SOPs which are Compliant for Inspections for a GXP Compliance" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance
Education: Education Technologies & Methods, Training
Health & Medicine: Medical laboratories, Medical technology, Pharma

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