Come engage with professionals from your local regulatory community over dinner and hear an interactive presentation on a particularly hot topic in the medical device industry. This event is coordinated by the RAPS Texas Chapter and is intended to encourage knowledge sharing and community development.
The Medical Device Single Audit Program (MDSAP) is a program that will allow the conduct of a single regulatory audit of a medical device manufacturer’s quality management system that will satisfy the requirements of multiple regulatory jurisdictions. Audits will be conducted by auditing organizations authorized by the participating regulatory authorities to audit under MDSAP. The MDSAP is a way that medical device manufacturers can be audited once for compliance with the standard and regulatory requirements of up to five different medical device markets: Australia, Brazil, Canada, Japan and the United States.
Don’t miss this unique opportunity to network with others from your region and to learn about the Medical Device Single Audit Program. A meal will be provided. RAC holders may claim 1.5 RAC recertification credits.
Contact RAPS Solutions Center at +1 301 770 2920, ext. 200, or email firstname.lastname@example.org to learn about the special student registration rate.