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Published in 2017 at "International Journal of Technology Assessment in Health Care"
DOI: 10.1017/s0266462317002215
Abstract: INTRODUCTION: Historically, patient access processes of new and innovative medical devices including in-vitro diagnostics are made in the sequence of regulatory approval, new Health Technology Assessment (nHTA) approval, reimbursement coverage and coding finally reaching the…
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Keywords:
access processes;
innovative medical;
patient access;
coverage ... See more keywords