QMSdesk

Input—per 1M tokens

Output—per 1M tokens

Context—tokens

WeightsClosed

About

QMSdesk is ranked #4 of 26 in document control software on Inferse. It runs on API, Web. There is no free plan.

Compared on document control software

Revision history: Yesqmsdesk.com
Approval workflows: Yesqmsdesk.com
Audit trail: Yesqmsdesk.com
Electronic signatures: Yesqmsdesk.com
Role-based access: Yesqmsdesk.com
Document expiry controls: Yesqmsdesk.com

Facts

Product: QMSdesk is a cloud eQMS for life sciences that connects quality processes in one system.qmsdesk.com · 2 Oct 2026
Modules: The pricing page says every tier includes eight core quality modules, including document management, quality events and CAPA, change control, training, risk, audits, supplier quality, and analytics.qmsdesk.com · 2 Oct 2026
Documents: Document workflows support Part 11 electronic signatures, controlled-copy watermarks, and cryptographic source-file hashing.qmsdesk.com · 2 Oct 2026
CAPA: Quality events supports seven event types, guided 5-Whys and Fishbone root-cause analysis, automated CAPA generation, and effectiveness checks.qmsdesk.com · 2 Oct 2026
Risk: The risk module provides dynamic FMEA scoring, severity escalation, drift detection, and cross-module traceability.qmsdesk.com · 2 Oct 2026
Integrations: The feature index lists SAML single sign-on with Okta, Microsoft Entra ID, Google Workspace, or custom SAML, plus a REST API with OAuth client credentials and API keys.qmsdesk.com · 2 Oct 2026
API limit: The feature index says API integrations can act but cannot sign electronic records.qmsdesk.com · 2 Oct 2026
Security: The maker says audit-trail entries are SHA-256 hash-chained, audit logs are insert-only, and tenant data is isolated with database row-level security.qmsdesk.com · 2 Oct 2026
Infrastructure: The homepage says QMSdesk is hosted on cloud infrastructure with a SOC 2 Type II attestation, and clarifies that the attestation belongs to the infrastructure provider, not QMSdesk.qmsdesk.com · 2 Oct 2026
Compliance: The platform is designed to support regulated use including 21 CFR Part 11, EU GMP Annex 11, and ISO 13485; the maker says customers file their own Part 11 §11.100(c) certification.qmsdesk.com · 2 Oct 2026
Validation: QMSdesk says its core platform is validated under a QA-approved Validation Summary Report, while each customer validates the system for its own intended use.qmsdesk.com · 2 Oct 2026
Audience: The early-adopter program targets life-sciences organizations including biotech, pharmaceutical, medical-device, IVD, CRO, CDMO, and testing-laboratory teams.qmsdesk.com · 2 Oct 2026
Implementation: The maker gives an 8–12 week target for a first working workflow, dependent on scope, data readiness, and team availability.qmsdesk.com · 2 Oct 2026
Support: The contact page says the quality engineering team responds to direct messages within four business hours and offers 30-minute tailored demos.qmsdesk.com · 2 Oct 2026
Maker: QMSdesk identifies itself as an Akatalyst platform; the site footer names Akatalyst Technologies Private Limited.qmsdesk.com · 2 Oct 2026