Validfor

Validfor

5.0 out of 5 stars
Docuply Validfor

Related Products

  • AlisQI
    4.5 out of 5 stars 108 Ratings
    Visit Website for AlisQI
  • SBS Quality Management Software
    5.0 out of 5 stars 7 Ratings
    Visit Website for SBS Quality Management Software
  • isoTracker Quality Management
    4.6 out of 5 stars 19 Ratings
    Visit Website for isoTracker Quality Management
  • Interfacing Integrated Management System (IMS)
    4.6 out of 5 stars 66 Ratings
    Visit Website for Interfacing Integrated Management System (IMS)
  • HR Partner
    4.7 out of 5 stars 205 Ratings
    Visit Website for HR Partner
  • Propel
    4.3 out of 5 stars 215 Ratings
    Visit Website for Propel
  • Process Street
    4.7 out of 5 stars 1,119 Ratings
    Visit Website for Process Street
  • QBench
    4.6 out of 5 stars 153 Ratings
    Visit Website for QBench
  • Intelex
    4.2 out of 5 stars 199 Ratings
    Visit Website for Intelex
  • Mitti (by SafetyCulture)
    4.6 out of 5 stars 872 Ratings
    Visit Website for Mitti (by SafetyCulture)
Docuply:

About

Docuply is a cloud-based electronic quality management system (eQMS) with integrated electronic document management and an electronic trial master file (eTMF) for clinical biotechnology companies, contract research organizations and other teams working in regulated drug development. It supports controlled document creation, review, approval, version tracking and electronic signatures, plus SOP training, deviation and corrective and preventive action (CAPA) workflows, supplier management, and trial-file organization using a CDISC TMF reference model. The platform provides audit trails, training records, document search and AI-assisted features for selected quality and document workflows. Teams can organize trial records and collaborate with external sites, sponsors and suppliers. Docuply is delivered as a web service hosted in the EU for GxP-related quality and clinical documentation processes.
Validfor:

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.
Docuply:

Platforms Supported

Windows Not Supported
Mac Not Supported
Linux Not Supported
Cloud Supported
On-Premises Not Supported
iPhone Not Supported
iPad Not Supported
Android Not Supported
Chromebook Not Supported
Validfor:

Platforms Supported

Windows Not Supported
Mac Not Supported
Linux Not Supported
Cloud Supported
On-Premises Not Supported
iPhone Not Supported
iPad Not Supported
Android Not Supported
Chromebook Supported
Docuply:

Audience

Clinical-stage biotech companies, small and medium-sized CROs, academic sponsors, and GxP service providers such as labs and biostatistics teams.
Validfor:

Audience

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

Support

Phone Support Supported
24/7 Live Support Not Supported
Online Supported
Validfor:

Support

Phone Support Not Supported
24/7 Live Support Not Supported
Online Not Supported
Docuply:

API

Offers API Not Supported
Validfor:

API

Offers API Not Supported
Docuply:

Screenshots and Videos

Validfor:

Screenshots and Videos

Docuply:

Pricing

€99/user/month
The free eDMS tier supports up to 8 users. The full eQMS plan is €99 per user/month for up to 50 users; larger-team pricing is also offered. A 14-day free trial is available. Optional SSO is priced separately.
Free Version Supported
Free Trial Supported
Validfor:

Pricing

No information available.
Free Version Not Supported
Free Trial Not Supported
Docuply:

Reviews/Ratings

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

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software
Validfor:

Reviews/Ratings

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

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.
Docuply:

Training

Documentation Supported
Webinars Supported
Live Online Supported
In Person Supported
Validfor:

Training

Documentation Not Supported
Webinars Not Supported
Live Online Not Supported
In Person Not Supported
Docuply:

Company Information

Docuply
Founded: 2022
Germany
docuply.io
Validfor:

Company Information

Validfor
Founded: 2024
Estonia
validfor.com
Docuply:

Alternatives

No Alternatives
Validfor:

Alternatives

Res_Q

Res_Q

Sware
Validfor:
Validfor:
Validfor:
Docuply:
Validfor:
Docuply:

Categories

Quality Management Supported
Validfor:

Categories

Docuply:

Integrations

Google Workspace Supported
Microsoft Entra ID Supported
Okta Supported
Validfor:

Integrations

Google Workspace Not Supported
Microsoft Entra ID Not Supported
Okta Not Supported
Docuply:
Claim Docuply and update features and information
Claim Docuply and update features and information
Validfor:
Claim Validfor and update features and information
Claim Validfor and update features and information