Featured Product In Quality
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
Quality
Increase Compliance, Reduce Risk with Integrated Digital Solutions – Webinar Recording/ Transcript
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Develop World-Class SOPs that Minimize Human Error – Webinar Recording/Transcript
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