{"id":73,"count":0,"description":"Here we go: on May 26, 2021, the Medical Device Regulation will become mandatory for all medical device manufacturers. Get free background information on the MDR now. Take the challenge into your own hands. We will be happy to support you by building up know-how, writing clinical approval documents, providing support as a remote team and\/or PRRC (responsible person for regulatory requirements according to Art. 15 MDR).","link":"https:\/\/mec-abc.de\/en\/products\/publications\/","name":"Publications","slug":"publications","taxonomy":"product_cat","parent":0,"meta":[],"_links":{"self":[{"href":"https:\/\/mec-abc.de\/en\/wp-json\/wp\/v2\/product_cat\/73","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/mec-abc.de\/en\/wp-json\/wp\/v2\/product_cat"}],"about":[{"href":"https:\/\/mec-abc.de\/en\/wp-json\/wp\/v2\/taxonomies\/product_cat"}],"wp:post_type":[{"href":"https:\/\/mec-abc.de\/en\/wp-json\/wp\/v2\/product?product_cat=73"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}