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A representative will be in touch with you shortly. While we process your request, please find additional information about the Medical Device Discovery Appraisal Program (MDDP) below.
Explore the ways organizations can
get started with MDDAP.
For answers to some technical questions see our list of FAQs and find a sampling of resources from ISACA, the FDA, and MDIC.
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CeloNova BioSciences, Inc.: Improving Operational Efficiency with ISACA’s CMMI MDDAP
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A program for medical device stakeholders to work together to enhance device quality and patient safety.
Program participants are eligible for regulatory modifications in the FDA’s pilot, which aims to elevate patient safety by leveraging CMMI as the framework by which medical device manufactures can measure their capability against best practices in a continuous improvement journey from compliance to quality.
Innovize has had a great experience going through the MDDAP assessment with experienced and well-trained assessors. The types of concerns found by the assessors provide a great roadmap to help Innovize improve our costs, efficiencies and achieve a higher maturity level.