Develop, manage, and oversee a single audit program that will allow a single regulatory audit to satisfy the needs of multiple regulatory jurisdictions
Clear Understanding of MDSAP objectives, approach and the overall process
To promote consistency, predictability, and transparency of regulatory programs
To promote greater alignment of regulatory approaches and technical requirements
How MDSAP Works?
What is MDSAP?
MDSAP Status
How does MDSAP fit with other certifications?
Next Steps in 2017 and going forward?
Beneficial to manufacturers of medical devices who are interested in marketing and selling devices in those countries (Regulatory Authorities)
Who should Attend
Clinical Project Managers
Clinical Research Associates
Clinical Investigators and Clinical Research
Regulatory Affairs Professionals
Regulatory Affairs Specialists
Regulatory Affairs Management
QA Auditors
Regulatory Project Leads/SME`s
GxP Auditors
Supplier Auditors
Clinical Affairs
Compliance Specialists
Quality Assurance
Quality Manager
Consultants
Production/Operations
Past Events
Implementing MDSAP (Medical Device Single Audit Program) for Compliance Success 2017 - 04-05 May 2017, Embassy Suites by Hilton Boston at Logan Airport, Massachusetts, United States (67338)
Important
Please, check "Implementing MDSAP (Medical Device Single Audit Program) for Compliance Success" official website for possible changes, before making any traveling arrangements
