Designing an Effective Cleaning Validation for Reusable Medical Devices in Today`s Regulatory Environment 2018

  • 12 Dec 2018
  • Webinar

Description

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today`s Regulatory Environment 2018 is an event dedicated to most current (regulatory) expectations for cleaning validation of reusable medical devices.

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today`s Regulatory Environment 2018 covers topics such as:

  • Cleaning validation design - manual cleaning.
  • Cleaning validation design - automated cleaning.
  • Choosing test soils.
  • IFU information to be supported.
  • Expectations for controls.
  • Choosing markers.
  • Report preparation.
  • Acceptance criteria selection.

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today`s Regulatory Environment 2018 intended for:

  • Validation specialists
  • QA personnel
  • R&D Personnel
  • Regulatory Affairs
  • Cleanroom Managers and Staff

Past Events

Important

Please, check "Designing an Effective Cleaning Validation for Reusable Medical Devices in Today`s Regulatory Environment" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device

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