Class I Medical Device Manufacturers Need an established QMS Under the New MDR
MedQdoc Resources:
Supporting Your Quality Management Journey
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.
Our resource pages include
Blogs and News
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.
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eQMS vs Paper-Based: Which Is More Cost-Effective?
Case studies
Read our case studies to learn how MedQdoc has helped medical device companies streamline their compliance processes and achieve regulatory success.
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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.
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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.
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Access our library of free resources and templates to support your medical device compliance journey.
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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.
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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.
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MedQdoc is used across the medical device industry
