Skip to site menu Skip to page content

Checklist: Supplier Documentation acc. to MDR 2017/745

By SIFo Medical

This free checklist shows ten points your suppliers must fulfil to comply with MDR 2017/745.

Not all points mentioned in the checklist are explicitly found in the regulations but are assumed and required by the authorities.

Download the checklist and ensure your suppliers comply with the Medical Device Regulation.

Enter your details below to view the free white paper

By downloading this whitepaper, you acknowledge that GlobalData may share your information with our white paper partners/sponsors who may contact you directly with information on their products and services.

Visit our Privacy Policy for more information about our services, how GlobalData may use, process and share your personal data, including information on your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Related Content