![]() Guidance on regulatory requirements for medical face masks How to verify that medical devices and personal protective equipment can be lawfully placed on the EU market and thus purchased and used – also in the COVID-19 context Guidance on state of the art of COVID-19 rapid antibody testsĬOVID-19 TESTS: Q&A on in vitro diagnostic medical device conformity assessment and performance in the context of COVID-19 (available in all EU languages and Arabic, Chinese, Japanese, Russian)Ĭonformity assessment procedures for protective equipment Notice to manufacturers and authorised representatives on the impact of genetic variants on SARS-COV-2 in vitro diagnostic medical devices Notice to 3rd country manufacturers of SARS-CoV-2 in vitro diagnostic medical devices Guidance on performance evaluation of SARS-CoV-2 in vitro diagnostic medical devices Summary of safety and clinical performance Guidance on clinical evaluation – Equivalence Guidance on sufficient clinical evidence for legacy devicesīackground note on the relationship between MDCG 2020-6 and MEDDEV 2.7/1 rev.4 on clinical evaluation Guidance on PMCF evaluation report template Guidance on safety reporting in clinical investigationsĪppendix: Clinical investigation summary safety report form Regulation (EU) 2017/745 – Questions & Answers regarding clinical investigationĬlinical evaluation assessment report template ![]() Instructions for generating CIV-ID for MDR Clinical InvestigationsĬlinical investigation application/notification documents Substantial modification of clinical investigation under Medical Device Regulation Guidance on content of the Clinical Investigation Plan for clinical investigations of medical devicesĬlinical Investigation Plan Synopsis TemplateĬommission Guidance on the content and structure of the summary of the clinical investigation report ![]()
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