Minerva PLM for Medical Device
This is the solution many companies have chosen to optimize their processes
From managing requirements, compliance, designs, and change management to traceability and reporting, Minerva PLM for medical device companies is a flexible PLM software solution. Minerva PLM is packed with out-of-the-box features that ensure quick software implementation time and access to proven capabilities that support your business processes.
More than 20 years of medical device industry experience is converted into industry best practice capabilities inside Minerva PLM. Take advantage of Minerva’s deep knowledge of the medical device industry and proven practices from previous implementations with other medical device companies.
Deep medical device industry knowledge put into best practice features inside Minerva PLM gives you several benefits as a business
- Save time on preparing and conducting audits
- Improve time-to-market for all products through deliverable driven project execution
- Automate the creation, maintenance and baselining of regulatory structures such as DHF, DMR and Technical File
- Fulfillment of medical device standards like 21 CFR Part 11 and FDA CFR 820
- Quick implementation due to out-of-the-box features
- Benefit from a subscription-based solution instead of a license model
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