Clinical Evaluation Report (CER) as a writing service

Clinical Evaluation Report

The Clinical Evaluation Report (CER) is an absolutely essential component of medical device regulatory submission. Changes to requirements imposed by MDR mean that it is more challenging than ever before to meet all regulatory obligations in drafting CERs and other regulatory documentation.

From enhanced requirements for clinical data to changes in rules on equivalence, CER writing is a task for experts with extensive experience in this field. We offer a full CER-writing service from conception to completion.

Our in-house expertise will allow us to translate information from an initial, structured client meeting into a document that meets the stringent requirement for CERs imposed by MDR.

Our expertise includes:

  • Clinical literature searching
  • Data summarisation
  • Drafting
  • Collating stakeholder input
  • Version control
  • Risk analysis summarisation

CERs require a high level of personnel time that is beyond the capacity of many companies working to ensure MDR Compliance. Let Mantra Systems be your partner in drafting CERs for your family of medical devices.

If you have any enquires or questions about our services, we'd love to hear from you.

If you have any enquires about our services, contact our team today.

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Our other Medical Device Regulation services

  1. Real World Evidence Generation Systems

    Real World Evidence Generation Systems

    We will design and deliver Real World Evidence (RWE) Generation Systems in the form of a Medical Device Product Registry that will enable your company to generate RWE in a way that complies fully with all relevant legislative and regulatory obligations including MDR, GDPR, ISO 13485, ISO 14971 and ISO 14155.

  2. Medical Risk Management for medial device manufacturers

    Medical Risk Management

    The publication of the new risk management standard BS EN ISO 14971:2019 - Application of risk management to medical devices outlines more stringent expectations for the performance of structured risk analysis than ever before.

  3. A Clinical Evidence Gap Analysis and research for MDR compliance

    Clinical Evidence Gap Analysis

    Ensure that expenditure on expanding your clinical evidence portfolio is targeted to those areas of most critical need. Our clinical expertise will identify important deficiencies in your clinical evidence portfolio and advise how to correct them in the most cost-effective manner possible.

  4. A Medical Complaints Handling service by healthcare professionals

    Medical Complaints Handling

    The effective processing of complaints is a central component of any effective medical device Quality Management System. Complaints are a crucial source of information about the performance of medical devices in real use and we will ensure they are handled to the highest professional standard.

  5. Post Market Surveillance Conduct

    Post-Market Surveillance conduct

    Our expertise in handling and assessing Medical Complaints, analysing clinical evidence gaps, performing risk analysis and building RWE Generation Systems allows us to be your holistic Post-Market Surveillance System generation partner.

  6. Clinical Competitor Analysis for medical device manufacturers

    Clinical Competitor Analysis

    A properly structured analysis of a competitor's clinical evidence portfolio can reveal opportunities for significant competitive advantage and can give indications as to where their products are failing to meet market expectations.

  7. Clinical Evidence Application Training for medical device manufacturer's sales teams

    Clinical Evidence Application Training

    Generating clinical data is expensive and time-consuming. While the primary objective in doing so may be to ensure MDR compliance of your devices, Mantra Systems can ensure that your sales team can effectively use this data to support sales calls.

Do you have any questions about our services?

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