Introduction to MDSAP Two Day Training Program
The Medical Device Single Audit Program allows an MDSAP recognised Auditing Organisation to conduct a single regulatory audit of a medical device manufacturer that satisfies the relevant requirements of the regulatory authorities participating in the program.
This global approach to auditing and monitoring the manufacturing of medical devices will improve their safety and oversight on an international scale.
Who Should Attend This Training:
This training is aimed at those with a working knowledge of a QMS from all levels within the organisation with responsibility for designing, implementing and maintaining Quality Systems including (but not limited to):
Quality Assurance – Quality Control Officers – Quality Managers
Regulatory Affairs – Other Departmental Managers – Quality Engineers
Internal Auditors and External Auditors