Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) 2016

  • 12-13 May 2016
  • Hilton Garden Inn Philadelphia Center City, PA, United States

Description

Topics
  • SOPs as part of the company`s regulatory infrastructure
  • SOPs and their relation to the regulations
  • Risk Based approach on SOP Best Practices for creation and maintenance
  • SOP on SOPs and how to ensure conciseness, consistency and ease of use
  • Tools for SOP tracking and when is validation required
  • Training on SOPs
  • What the FDA looks for in SOPs during an inspection
Who should Attend

Senior attendees from:

  • Clinical Affairs
  • Regulatory Affairs
  • Compliance
  • Quality Assurance/Quality Control
  • Manufacturing and Technical Services
  • Marketing & Sales
  • IT/MIS
  • Engineering
  • Laboratory Operations
  • Executive Management
  • Clinical Research managers and personnel
  • Customer Service
  • QA/RA managers and personnel
  • Specialists/SMEs in all departments
  • Distributors/Authorized Representatives
  • Quality System auditors
  • Consultants
  • Legal Counsel

Past Events

Important

Please, check "Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
Science: Life Sciences & Biology
Technology: Biotechnology

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