Index
A
performance characteristics, 201
schematic illustration, 201
accelerators, 412
accelerometers, 344
active device surface, 86–91
general issues, 86–7
active implantable medical devices
approval process, 314–20
bench testings, animal studies and human clinical trials, 315–20
CE marking and FDA approval, 320
progressive tests series, 316
required steps, 315
development in regulated environment, 299–323
future trends, 322–3
maintaining feedback from market, 321
medical device, 303–8
quality management system (QMS), 308–14
route to market, 300–3
product life cycle, expectations and risk sharing, 301–2
project planning, 302–3
simple ...
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