Benefit from the unique knowledge and insight of our MDR-trained professionals. Aimed at suppliers and manufacturers of medical devices from across the industry, this training webinar will give you an empowering perspective on working successfully with the MDR.
1. Get beneath the skin of the EU MDR and understand the key requirements for medical device regulatory compliance.
2. Build active regulatory systems that will safeguard your MDR transition through targeted knowledge and understanding.
3. Learn the secrets to generating, identifying, appraising and analysing clinical evidence for medical device compliance.
4. Access powerful resources and personal support that will complement your internal capabilities in working with the MDR.
The slides from this webinar can be downloaded here:
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For more information on our services, please visit:
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We recommend visiting our MDR Compliance guide section of the website for FREE content on how to conduct Clinical Evaluation effectively as well as utilising the best procedures for writing Clinical Evaluation Reports.
Clinical Evaluation:
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Clinical Evaluation Report writing:
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