Mantra Systems
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EU/UK MDR Market Access Masterclass - December 2023
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MDR Annex II Templates - Produce MDR Annex II technical documents for your medical devices
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MDR Risk Management training course - Build, document & maintain an ISO 14971:2019-compliant system
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MDR CER Writing training course - Learn the secrets of our Clinical Evaluation process
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Clinical Evaluation Plan Template - Produce EU MDR-compliant CEPs for any class of medical device
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MDReady Starter Guide - A free step-by-step guide for your journey to MDR compliance
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Clinical Evaluation Report Template - Produce EU MDR-compliant CERs for any class of medical device
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Clinical Evaluation - Medical device CERs, CEPs, literature reviews & data analysis
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Online medical affairs training courses & alternative, non-clinical career opportunities for doctors
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What is Post-Market Surveillance (PMS) in the EU MDR?
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How to build a winning strategy for EU MDR Compliance & Medical Device Regulatory requirements
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MDR Gap Analysis Tool - Perform a Gap Analysis on your medical devices for EU MDR Compliance
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How to work with Annex VIII from the Medical Device Regulation (EU MDR)
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How to work with Annex I from the Medical Device Regulation (EU MDR)
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