MedQdoc Resources:
Everything you need for compliant Quality Management

Templates, videos, case studies and guidance to help you work paperless with QMS and technical documentation.

MedQdoc resources support compliant, paperless QMS and technical documentation across ISO 13485, MDR/IVDR and FDA requirements.

ISO 13485:2016
Certified

Validated
eQMS solution

21 CFR Part 11
Compliant

This resource hub brings together documentation templates, introduction videos, case studies and expert insights — all created to help medical device companies build and maintain a structured, fully paperless QMS and technical documentation.

Our resource pages include

Introduction Videos

Start here to get a clear overview of how MedQdoc works and how to get started with a structured, fully paperless QMS and technical documentation.

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Introduction and start page overview of MedQdoc eQMS

Introduction to MedQdoc

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Creating a technical document and sending it for review in MedQdoc eQMS

Technical Documentation with MedQdoc

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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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Building Quality as a Team Effort – How Klavant prepares for ISO 13485 with MedQdoc

Customer Survey Highlights

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.

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.

Downloads

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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Next steps

Request a MedQdoc Demo

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Medical Device eQMS

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