Simplifying Global Compliance
Featured Product In Medical Devices
Biological Risk Evaluation and Management for Medical Devices
$397.00
Report shows how the FDA incorporates the two ISO standards in its medical device development policy, how the EU version of the two standards differs in significant ways and how the EU Medical Device Regulation may require further changes in the European standards. Read More
Medical Devices
Medical Device Voluntary Malfunction Disclosure Regulation - Webinar Recording/Transcript
$287.00
Medical Device Cybersecurity Risks & Best Practices - Webinar Recording/Transcript
$287.00
Laboratory Developed Tests, In Vitro Diagnostics & Gene Therapies - Webinar Recording/ Transcript
$287.00
Brexit and the Impact to Your Global Business Operations - Webinar Recording/Transcript
$287.00
De Novo Strategies for Getting Your Medical Device Approved - Webinar Recording/ Transcript
$287.00
