21 CFR Part 11 compliance for software validation and SaaS/Cloud 2019

  • 2019

Description

Topics
  • Avoid 483 and Warning Letters
  • What is expected in Part 11 and Annex 11 inspections
  • A computer system using risk-based validation to gain maximum productivity and reduce cost by as much as two thirds
  • How to buy COTS software and qualify vendors
  • How to select resources and manage validation projects
  • Requirements for local, SaaS, and cloud hosting
  • Minimize the validation documentation to reduce costs without increasing regulatory or business risk
  • "Right size" change control methods that allows quick and safe system evolution
  • Protect intellectual property and keep electronic records safe
  • Test cases that trace to elements of risk management
Who should Attend

Attendees from:

  • All GxP system users
  • QA, IT, management

Past Events

Important

Please, check "21 CFR Part 11 compliance for software validation and SaaS/Cloud" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Management, Quality assurance
Health & Medicine: Healthcare
Technology: Information Technology (IT)

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