Verification vs.Validation-Product,Process or Equipment and QMS Software 2018

  • 15 Aug 2018
  • Webinar

Description

Verification vs.Validation-Product,Process or Equipment and QMS Software 2018 is a webinar that covers topics such as:

  • The Project V&V Plan
  • Verification or Validation-FDA Expectations
  • Product and Process/Test Facilities/Equipment Software V&V
  • An FDA-accepted Documentation "Model"
  • The FDA`s 11 Key V&V Documentation Elements
  • When and How to Use DQ, IQ, OQ, PQ (or their equivalents)
  • IEC 62304,GAMP/Other Considerations
  • "White Box" and "Black Box" Validations

Verification vs.Validation-Product,Process or Equipment and QMS Software 2018 is intended for:

  • QA / RA
  • Senior management in Drugs,Devices,Combination Products,Biologics,Dietary Supplements
  • R&D
  • Software development,Programming,Documentation,Testing teams
  • Production
  • Engineering
  • Consultants,Others tasked with product,Process,Electronic records software V&V responsibilities
  • Operations

Past Events

Important

Please, check "Verification vs.Validation-Product,Process or Equipment and QMS Software" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Science: Engineering
Technology: Information Technology (IT), Software & Applications

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