Medical Device Document Writing – Correct Knowledge Process Outsourcing Partner will Be the Next-Gen Key to Success

Ashish Indani
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Ashish Indani: Complementary and Alternative Medicine, India

Current Trends in Biomedical Engineering & Biosciences, 2017, vol. 1, issue 4, 86-89

Abstract: The medical device regulation is constantly evolving along with the evolving biomedical technology. Recently added guidance on 3D printed devices and customized medical implants in US, amendments in the Clinical Evaluation Report guidelines, Medical Device Reporting guidelines in EU and China and introduction of medical device rules 2017 in India are three major examples of the regulation’s efforts keeping up with the technology.

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Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:adp:jctbeb:v:1:y:2017:i:4:p:86-89

DOI: 10.19080/CTBEB.2017.01.555568

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