The transition from EU MDD (2007) to EU MDR (2017) has included an increase in expectations for...
Is your business challenged by a complex and ever changing global regulatory environment? Medpoint can help!
Preparing your business to be compliant to game changing requirements can be overwhelming. Medpoint has experts that can help you assess, plan, and implement strategies to effectively and efficiently stay ahead of emerging regulations and standards. Prepare your organization for Medical Device Single Audit Program (MDSAP), updated standards such as ISO 9001 and ISO 13485, and new EU device and IVD regulations with the Medpoint team by your side. Contact us today: hello@medpoint.com or 800.200.9292.
