# VLMcare

> Data-driven, AI-enhanced validation for regulated life sciences. Connected requirements, tests, approvals, and audit-grade traceability.

## About

VLMcare is electronic Validation Lifecycle Management (eVLM) software for regulated
life sciences companies: pharmaceutical manufacturers, biotech, medical device makers,
CDMOs, CROs, hospitals, and laboratories.

Instead of managing validation as a pile of documents, VLMcare manages it as structured
data. Requirements, risks, test scripts, results, deviations, and approvals are objects
that stay connected, so traceability and audit evidence are generated as work happens
rather than assembled afterwards.

Scope covers Computer System Validation (CSV), Commissioning, Qualification and
Validation (CQV), process validation including Continued Process Verification (CPV),
laboratory instrument qualification, and periodic review. The platform is built to
support GxP requirements, GAMP 5, EU Annex 11, FDA 21 CFR Part 11, and GDPR.

VLMcare is part of QbD Group and runs on the Microsoft stack. The company is certified
to ISO/IEC 27001:2022 and ISO 9001:2015. Offices are in Newport Beach, California (US)
and Antwerp (Belgium). Sibling product: IFUcare.

Tagline: "Validation Lifecycle Management, with care."

## Pages

- [Home](/): Validation Lifecycle Management — data-driven, AI-enhanced, audit-ready validation software for regulated life sciences.
- [Product](/product): Overview of the VLMcare platform, its architecture, and how it connects requirements, tests, and approvals.
- [Capabilities](/capabilities): Detailed capability areas including validation planning, test management, document control, and audit readiness.
- [Why eVLM](/why-evlm): The case for electronic Validation Lifecycle Management over paper-based or legacy approaches.
- [Customers](/customers): Customer stories and outcomes from life sciences organizations using VLMcare.
- [Resources](/resources): Articles, guides, and insights on validation lifecycle management best practices.
- [Continued Process Verification Guide](/resources/continued-process-verification): Practical guide to CPV (Stage 3 process validation) and the move from PQ to data-driven CPV monitoring.
- [Journal](/blog): Validation field notes — ideas, reactions, and news for quality and validation professionals in life sciences.
- [Trust Center](/trust-center): Security controls, ISO/IEC 27001:2022 and ISO 9001:2015 certifications, GxP compliance, GDPR posture, and downloadable assurance documents.
- [Request Demo](/contact): Schedule a demo or get in touch with the VLMcare team, including office locations.
- [Rescop Customers](/rescop-customers): Information for Rescop customers transitioning to VLMcare.
- [Cookie Policy](/cookie-policy): How VLMcare uses cookies and manages consent.

## Journal articles

- [VLMcare Implements a Full CSV, CQV, and Instrument Validation Program in 6 Weeks](/blog/full-csv-cqv-instrument-validation-6-weeks): Go-live of a complete CSV, CQV, and lab instrument validation implementation for a major US personal care medicine company, delivered in six weeks.

## Machine-readable

- [Sitemap](/sitemap.xml)