Plumely

Every tool your team needs — nothing you don’t

Sign up as an organization, then turn on individual tools and assign each one to the roles and users who need it. No bundled suite, no features you have to work around — just the tools relevant to your team, activated one at a time.

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Supplier & CoA Qualification

Verify every incoming batch has an in-spec, non-expired CoA from a qualified supplier before it reaches your line.

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Country Dossier Checklist

Living, country-specific dossier checklists for CTD, ACTD, and Module 1 requirements across emerging markets.

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Export Documentation & Compliance

CoAs, CoPPs, WHO-GMP certificates, and shipping documents — tracked, versioned, and never expired without warning.

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RLD / Orange Book Comparator

Follow reference-listed drugs for label, patent, and exclusivity changes without checking the FDA site by hand.

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Protocol Amendment Impact Checklist

Turn a protocol amendment into an owned, tracked checklist across every affected system and document.

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Deviation & CAPA Tracker

Mobile-first deviation logging and CAPA tracking built for the shop floor, not just the QA office.

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Stability Study Tracker

Pull-point calendars, sample inventory, and overdue-test alerts for every active stability study.

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Clinical Trial Lite Manager

Protocol tracking, enrollment logs, and essential-document checklists sized for a 1-3 study site.

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