Olympus + ASP Collaborative Conversation Webinar

Patient Safety First: The Importance of Proper Device Validations to Reduce the Risk for Infection

This collaborative webinar features a panel discussion on device validation between industry leaders in endoscope manufacturing and sterilization solutions.

Learning Objectives

  • Identify various guidelines, standards and regulations affecting the validation process
  • Describe elements of the device validation process
  • Discuss the manufacturer’s roles and responsibilities for determining efficacy and durability
  • Identify how the validation process impacts infection prevention and control

To learn more about the device validations process at ASP or to speak to one of our sterilization experts, contact ASP today.

Are you a medical device manufacturer?
Contact the Technical Business Solutions team at [email protected] to learn more about our corporate partnership program.

Acknowledgement

ASP is committed to the ethical collaboration and interaction with Healthcare Professionals. Under the Open Payments Act, also known as the Sunshine Act, ASP is required to report payments or transfers of value for expenses associated with this event, if applicable.

All content of this presentation is owned by their authors and its protected by worldwide copyright laws.

AD-210141-01-CT_A-MDR