In-Vitro Diagnostics 2017

Topics

• What does the future hold for companies of the In-Vitro Diagnostics industry
• Update on the In-Vitro Diagnostic regulation
• The increased requirements for post market surveillance
• How the change in classifications will impact industry with UL
• The implementation of the Qualified Person (QP)
• The Medical Device Single Audit Program (MDSAP)

Who should Attend

In-Vitro Diagnostic manufacturers, regulators, diagnostic companies.