Plumely
Built for pharma & API manufacturing teams

Built for Manufacturing Teams.
Specialized for Pharma & API.

One platform. Every compliance tool your team actually needs.

Stop stitching together spreadsheets, email, and enterprise QMS modules you don't need. Activate the tools your organization actually needs, assign them to the right roles, and leave the rest switched off — cloud-hosted or running on your own infrastructure.

Audit-trail & e-signature controls built for GxP records
HIPAA & GDPR-ready architecture
Cloud or self-hosted on your own Postgres
Overview

One tool library.
Built for the whole team.

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Compliance Tools

One library, spanning supplier qualification to stability tracking.

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Countries in the Dossier Library

India, Philippines, Kenya, the UAE, and Brazil — more added as they're built out.

Append-only

Audit Trail

Every mutation is hash-chained to the one before it — not even an admin can edit or delete it after the fact.

The tool library

One login. 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 CRM, no features you have to work around.

Available now

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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Available now

Country Dossier Checklist

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

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Available now

Export Documentation & Compliance

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

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Available now

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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Available now

Protocol Amendment Impact Checklist

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

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Available now

Deviation & CAPA Tracker

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

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Available now

Stability Study Tracker

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

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Available now

Clinical Trial Lite Manager

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

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Try it now

Five tools you can use right now — no account required.

These pull real, live public data. Everything else needs an organization, since it's tracking your own records — these don't, so try them first.

RLD / Orange Book Comparator

Live search against FDA's public Orange Book — no account needed.

FDA Drug Recall Lookup

Live search against FDA's public enforcement/recall database — no account needed.

Clinical Trials Search

Live search against the official ClinicalTrials.gov registry — no account needed.

Country Dossier Checklist

Browse our curated dossier requirement library — free, no account needed.

Brazil (ANVISA)CTD
3 required documents tracked
India (CDSCO)CTD
4 required documents tracked
Kenya (PPB)CTD
3 required documents tracked
Philippines (FDA)ACTD
4 required documents tracked
United Arab Emirates (MOHAP)CTD
3 required documents tracked
Sign up to start a dossier and track document status →

Export Invoice Currency Converter

Live ECB reference rates for commercial invoices — no account needed.

Browse all free tools on their own pages →