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About

Batch records, cleaning, environmental monitoring & inventory management. Optimize advanced therapy production with software designed for GMP. It’s one more way to align your workforce for ‘right-first-time manufacturing’. Get rid of fragmented paperwork
with one software that everyone can use for data collection, review & approval workflows, reporting, and analytics. Ensure your team follows the
correct steps in due time to enable the right manufacturing with interactive work instructions. 21 CFR part 11 and EU Vol 4 annex 11 compliant for your peace of mind. Make logging information intuitive with bar code scanning, built-in data integrity checks, and automated calculations. Highlighting out of specs and review by approval comes built-in. Know where your samples are in the testing process. Organize sample plans and automate trending. Know where your samples are in the testing process. Manage tasks to keep cleanrooms clean and track any production process.

About

Validfor is a secure, modular digital validation platform that centralizes the entire validation lifecycle on a single, paperless system. Designed specifically for regulated industries, Validfor enables efficient validation while ensuring full compliance with GAMP 5, 21 CFR Part 11, and EU Annex 11. The platform supports electronic records and advanced electronic signatures with full audit trails, role-based workflows (Author, Reviewer, Approver), and complete CSV compliance. All documents and records are securely managed in a centralized repository, capturing every change with full traceability to protect data integrity and Quality Assurance. Validfor offers integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, enabling seamless impact assessments, CAPA tracking, Computer Software Assurance (CSA), and audit-ready lifecycle management.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Biopharmaceutical companies seeking a tool to improve the digitalization of their regulated laboratory and cleanroom workflows

Audience

Primary: Pharmaceutical & Life Sciences Companies Quality Assurance & Validation Teams Secondary: Regulated Manufacturing Organizations Compliance & CSV Professionals GxP-regulated Enterprises

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

No information available.
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

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Reviews/Ratings

Overall 5.0 / 5
ease 4.0 / 5
features 5.0 / 5
design 5.0 / 5
support 5.0 / 5

Pros & Cons from Real Users

Pros

  • Strong audit trail mindset and a clean approval workflow. I like that evidence stays attached to the work items it belongs to, which makes audit narratives easier.

Cons

  • I want more guardrails/templates for teams new to VLM so they don't invent inconsistent structures across departments. Also would like more flexible approval routing patterns for complex orgs.

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

MyCellHub
Founded: 2019
Belgium
www.mycellhub.com

Company Information

Validfor
Founded: 2024
Estonia
validfor.com

Alternatives

Alternatives

DELMIAworks

DELMIAworks

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Lockbox LIMS

Lockbox LIMS

Third Wave Analytics

Categories

Categories

Integrations

No info available.

Integrations

No info available.
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