Medical Device Single Audit Program: Fundamentals
Gain the knowledge and skills required to successfully host a MDSAP audit within your organization.
Obtain in depth knowledge about this new type of audit and how your organization is best prepared to support the completing of requirements within the allotted time.
Discover how this program differs from the traditional ISO 13485 through its regulatory audit approach, the grading of nonconformities, and handling of the audit report.This course will prepare you to host a MDSAP audit and allow you to determine if your own internal QMS processes are consistent with the requirements of the MDSAP audit mode for the jurisdictions where your products are marketed.
Upon completion of this training, delegates will be able to support their organization to maintain compliance to ISO 13485 and jurisdiction requirements in the countries engaged in the MDSAP program.