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General principles of GDPR and actions manufacturers can take to gain or maintain compliance.
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Secure data management to meet HIPAA, GDPR requirements and achieve regulatory compliance.
Use this short checklist to assess what your medical device company needs to do to comply with the EU MDR.
Gain insights into Human Factors Engineering (HFE) and medical device design with this list of publications.
This brief checklist will help you to determine how to bring your in vitro diagnostic medical device company into compliance with the EU IVDR.