Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes 2017

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes 2017 is a conference that covers topics such as:

• Device Classification
• The Medical Device Single Audit Program (MDSAP)
• Medical Device GMP
• Licensing Pathways
• Device Labeling
• Inspections
• Timelines and Fees
• License Holder Responsibilities
• Adverse Event Reporting
• Country Specific Cultural Considerations and Challenges

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes 2017 is intended for all personnel in the Medical Device industry.