Expert compilation, review, and remediation of EU MDR 2017/745 Technical Documentation. Ensure your dossier is audit-ready for Notified Body submission
Medical device manufacturers placing products on the European market must prepare and maintain comprehensive technical documentation to demonstrate compliance with the EU Medical Device Regulation (MDR) 2017/745.
A CE Marking Technical File is a core regulatory requirement for medical devices and provides the documented evidence needed to demonstrate that a device meets the applicable General Safety and Performance Requirements (GSPRs).
Patient Guard provides expert CE Marking Technical File services for medical device manufacturers, supporting the preparation, review, remediation, and ongoing maintenance of MDR-compliant technical documentation.
We help manufacturers build structured, audit-ready Technical Files that align with MDR Annex II and Annex III requirements and support notified body review where applicable.
Whether you are preparing a new Technical File, updating legacy documentation, or addressing identified gaps, we ensure a clear and compliant route to CE marking readiness.
Under Regulation (EU) 2017/745, manufacturers must prepare and maintain technical documentation that demonstrates conformity with the applicable requirements of the MDR.
A compliant Technical File for a medical device typically includes:
| No | Heading | Contents |
|---|---|---|
| 1. | Device Description | Full specifications, intended use, and UDI-DI |
| 2. | Labelling & IFU | Instructions for use in all required EU languages. |
| 3. | Design & Manufacturing | Documentation of design stages and supply chain sites. |
| 4. | GSPR Mapping | Evidence for General Safety and Performance Requirements. |
| 5. | Benefit-Risk Analysis | Full risk management files (ISO 14971) |
| 6. | Verification & Validation | Bench testing, sterilization, biological evaluation, clinical evaluation |
| 7. | Post Market Surveillance | PMS Plan, PSUR, PMCF Plan, PMCF Reports |
Is your CER MDR-compliant? Under the latest MDR standards, clinical evidence must be proactive and continuous. We ensure your Technical File contains a robust Clinical Evaluation Report supported by your Post-Market Surveillance (PMS) data.
If your device incorporates AI or machine learning, your technical documentation must now address the requirements of the EU AI Act. We specialize in mapping software lifecycle processes (IEC 62304) and cybersecurity measures into your CE dossier.
We assess your device, classification, and current documentation status.
We review your existing Technical File or source documents against MDR requirements.
We identify missing sections, weak justifications, and documentation gaps.
We help compile, revise, and structure the Technical File for compliance.
We support final checks ahead of submission, audit, or notified body review.
We support Technical File preparation for a wide range of medical devices, including:
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Ensure regulatory compliance and market readiness with expertly prepared CE Marking Medical Device Technical Files. Pricing starts from £6,000, with preferential rates for multiple products.
Assessment of your device and existing documentation against MDR Annex II & III requirements.
Compilation, structuring, and correction of documentation including GSPR, risk management, and clinical data.
Final compliance check and preparation for Notified Body review or EU market placement.
Fast turnaround: most Technical Files are delivered within 4–8 weeks, subject to completeness of product information.
A CE Marking Technical File is the set of technical documentation required to demonstrate that a medical device complies with the applicable requirements of the EU Medical Device Regulation (EU) 2017/745.
Yes, all medical devices placed on the EU market require technical documentation. The scope and complexity depend on the device classification, intended purpose, and applicable conformity assessment route.
A Technical File typically includes device description, design and manufacturing information, risk management, GSPR compliance, verification and validation data, clinical evaluation, labelling, and post-market surveillance documentation.
Yes, we can review your current Technical File, identify compliance gaps, and help remediate the documentation to align with MDR requirements.
Timelines depend on the complexity of the device and the availability of supporting documentation. Where the source documentation is already available, review and remediation can begin immediately.
Click on the links below to discover more:
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Medical devices exist to improve health outcomes, but every device carries potential risk. Managing those risks in a structured, documented, and defensible way is essential for regulatory approval and patient safety.
Clinical evidence is central to demonstrating the safety and performance of medical devices in the European Union.
Medical device labelling is more than a packaging exercise. It is a regulatory requirement that communicates essential information about a device’s identity, safety, and intended use.
Regulatory approval is not the end of scrutiny, it is the beginning of structured data collection.
If you are implementing a medical device QMS, preparing for certification, or recovering from audit findings, understanding ISO 13485:2016 requirements is non-negotiable.
Speak to one of our regulatory and compliance experts to arrange an obligation-free call. Our experienced team is ready to help you get your medical device to market.
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For help with the checklist or other aspects of your compliance journey, please reach out to us at Patient Guard and our experts would be happy to help.
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For help with the checklist or other aspects of your compliance journey, please reach out to us at Patient Guard and our experts would be happy to help.
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