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Jama Connect for Medical Device & Life Sciences
Evidence strength: Moderate How this is scored
Requirements, risk and V&V platform for medical device and life-sciences teams. Official frameworks list includes Medical Software Development: IEC 62304, plus FDA 21 CFR 820.30, EU MDR and ISO 14971. Suitably validated by TÜV SÜD for safety-related development. Not an FDA PCCP product.
Certification evidence
Maps to 1 IEC 62304 requirement — see which with Pro
Certification relevance. Cited pages map this listing to IEC 62304 (1 requirement).
Cited page: Jama Software: Medical Device/Life Sciences Development Software | Jama Connect — a named IEC 62304 requirement.
Cited page · The quoted wording is Pro.
Listing detail and source evidence (Pro)
Included on Pro, Team and Enterprise. Public summaries, tags and official links on this page stay free.
Cited mappings (Pro)
Included on Pro, Team and Enterprise. Public summaries, tags and official links on this page stay free.
Procurement evidence pack (Pro) — print cited mappings and analyst notes. The print view is not on this page.
- Vendor / publisher
- Jama Software
- Type
- Commercial
- Official site
- https://www.jamasoftware.com/solutions/medical-device/
- Industries
- Frameworks named on cited source
- Last verified
Listing is not an endorsement, certification or recommendation. Capabilities, availability and framework support can change. Confirm with the vendor and the relevant authority. See the disclaimer.