Compliance, Verification, and Validation are critical to the medical industry and validation is important regardless of the area; process, clean room, sterilization, equipment or method validation are important to make sure your product is reproducible, safe, cost-effective and risk is appropriately managed.
Non Product Software Validation is a challenging area and SSI will have a conversation with an industry SME, Tom Bento on what defensible compliance is, critical thinking and your checklist for Validation of NPS and defining the entire scope of what Validation of Non Product Software should look like.
Don't miss this critical opportunity to learn from a SME on a challenging area of compliance in the medical industry.
a. What does Simplified, Defensible Compliance mean?
b. Checklist Vs Critical Thinking for Validation of NPS
c. Understanding and Defining the Scope of NPS Validation
Thomas is currently the Principle consultant at Verity Compliance LLC, working shoulder to shoulder supporting Medical Device Manufacturers in Simplified, Defensible Compliance Strategies. He has been in the regulated space for more than 17 years...