- 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?
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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.