How to build a winning strategy for EU MDR Compliance & Medical Device Regulatory requirements

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:
sowl.co/3cADv
For more information on our services, please visit:
www.mantrasystems.co.uk/medic...
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:
www.mantrasystems.co.uk/eu-md...
Clinical Evaluation Report writing:
www.mantrasystems.co.uk/eu-md...
** Please like and share the video to help our channel to grow. Also, leave a comment - let us know what areas of the MDR you are struggling with and we will try and answer as many questions as we can. It also will help us create future content for you. **
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[@timglover4180]

Brilliant webinar! Exactly what I’ve been looking for! Thank you

[@kdjain]

Thumbs up! Excellent slides and explanation.

[@mantrasystems]

Much appreciated! We are glad you found it rewarding.

[@carolankenau4222]

Hi! thanks a lot, could you share me the pdf?

[@mantrasystems]

Hello Caro. The slides from our webinar can now be downloaded here: sowl.co/3cADv