eQMS Tools & Resources for the Medical Device Industry

Whether you are aiming for ISO 13485 certification and/or to ensure QSR, ISO 14971, MDR/IVDR compliance to get your medical device CE-marked or successfully registered to any other market, these materials are designed to help you.

This resource page includes information on the documentation templates available via MedQdoc, as well as case studies and blog posts to provide you with further inspiration and support on your medical device compliance journey.

Tools and Downloads

Case Study

MedQDoc ISO 13485 Case Study: Aidee

Aidee Health are a MedTech start-up that needed an eQMS to help them navigate the regulatory requirements of the industry to bring their innovative blood pressure monitor to market.

Document

MedQdoc MDR Technical Document Templates

Discover the range of MDR technical document templates available via MedQdoc to support your compliance with the Medical Device Regulation (EU) 2017/745.

Download

Document

MedQdoc IVDR Technical Document Templates

Explore the different IVDR technical document templates available in MedQdoc to support your In Vitro Diagnostic Medical Device Regulation (EU) 2017/746 compliance.

Download

Document

MedQdoc QMS Templates

Learn about the huge variety of QMS templates available through MedQdoc, to help you on your ISO 13485 and QSR journey.

Download

Case Study

MedQDoc ISO 13485 Case Study: NORBIT

Discover how MedQdoc enabled NORBIT to achieve ISO 13485 certification for manufacturing of medical devices in just six months.

Case Study

MedQdoc eQMS Case Study: Inossia

Medical device company Inossia wanted to achieve ISO 13485 certification and QSR compliance as part of the process for bringing their new product to market.

Demonstration

MedQdoc demonstration

Request a no-obligation MedQdoc demonstration with one of our regulatory compliance specialists to find out how MedQdoc could deliver value to your business.

Book Demo

Blogs

Read the latest articles by our quality and regulatory specialists, for a more in-depth look at different aspects of medical device industry regulatory compliance.