Clinical Evaluation of European Medical Device Regulations (MDR) Training Course (ONLINE EVENT: July 21-22, 2025) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Training Course" training has been added to ResearchAndMarkets.com's offering.

This introductory course will cover all aspects of clinical evaluation in line with the European Medical Device Regulation (MDR) and applicable guidance documents.

The programme will provide you with the tools and skills you will need to produce a high-quality clinical evaluation report (CER) for all your medical devices. You will understand the detail of what clinical data is needed, how to collect it, analyse it and receive direction on producing a CER that is acceptable to the regulatory authorities and Notified Bodies. You will learn how the process fits into the development of a medical device and also the post-market aspects of clinical evidence.

The programme includes case studies and template documents which you will be able to utilise to produce your own clinical data evidence documentation.

Benefits of attending

• Gain a detailed overview of the clinical evaluation process
• Understand the concepts involved in conducting a clinical evaluation
• Learn how to utilise information gathered during a clinical evaluation
• Take away skills in conducting systematic literature searches
• Understand where clinical evaluation fits into the development and marketing of medical devices
• Explore how to appraise data
• Know how to assemble clinical evidence acceptable for review by regulatory authorities or Notified Bodies

Certifications:

• CPD: 12 hours for your records
• Certificate of completion

Who Should Attend:

• CROs
• Medical writers
• Clinical staff
• Those who conduct clinical evaluations/investigations/post-market follow-up studies
• Those moving from pharmaceuticals to medical devices

And personnel involved in:

• Gathering clinical evidence and conducting clinical evaluations
• R&D
• Regulatory affairs

Key Topics Covered:

What is a clinical evaluation?

• Explanation of the terminology used in clinical evaluations
• Overview of a clinical evaluation
• The importance of clinical evidence in medical device development

Why and when is it necessary to conduct a clinical evaluation?

• Where does clinical evaluation sit within the medical device process?
• Why is clinical evidence important?
• Who are the stakeholders in the process?

Who and what is involved in the clinical evaluation process?

• Overview of each step
• Use of equivalent products

Workshop: bringing it together

• An interactive exercise on what has been learnt so far

What regulations govern clinical evaluations and what guidance documents should clinical evaluations be conducted to?

• An in-depth review of the available regulatory and guidance documents which can be utilised during the process and how to interpret these

Documentation necessary for conducting a clinical evaluation

• The clinical evaluation plan

The literature review process

• Selecting databases and conducting searches
• How to source data and review it
• How to clarify the question on which you need to find literature, including devising the most comprehensive literature search strategy and selecting keywords

The Clinical Evaluation Report (CER)

• What is it and what is included?
• Who should write it?
• How to write it

What is state of the art and how to conduct a risk benefit assessment of the data?

• Performance and safety analysis
• State-of-the-art analysis
• Risk-benefit analysis

Impact of the Medical Device Regulations (MDR)

For more information about this training visit https://www.researchandmarkets.com/r/284j94

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