Liu C(1), Shi Y(1), Hou L(1), Sun X(1). Author information:
(1)Shandong Quality and Inspection Center for Medical Devices;NMPA Key
Laboratory for Quality Control of Pharmaceutical Packaging;NMPA Key Laboratory
for Quality Control of Pharmaceutical Packaging;Shandong Provincial Key
Laboratory of Biological Evaluation for Medical Devices, Jinan, 250101.
To broadly understand the new direction of biological evaluation for medical devices, we introduced both domestic and international progress of biological evaluation and focused on illustrating the key points on full life-cycle biological evaluation, toxicological risk evaluation, evaluation endpoints and package material evaluation concern as well as how to use the update vision of ISO 10993-1:2018 scientifically and reasonably in order to provide us better services on performing biological evaluation for medical devices.
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