We help life science companies automate their validation testing & documentation
Reduce manual effort. Accelerate releases. Reclaim time.
Benchmarks based on similar work. Results vary by scope, tools, and complexity.
Benchmarks based on similar work. Results vary by scope, tools, and complexity.
We help life science companies automate their GxP validation testing and documentation, aligned with GAMP 5, FDA CSA, and Annex 11. Validation experts focus on judgment and oversight while the automation handles execution, evidence collection, and document compilation.
Automate environment setup, test data preparation, and execution sequencing to reduce manual effort, coordination and rework.
Automatically generate consistent test evidence, and compile it into controlled validation documents via rule-based template population.
Route exceptions and generated documents to qualified reviewers for expert review and approval, reducing QA loops while maintaining clear traceability and human-in-the-loop controls. Final authority remains with your validation team.
Schedule regression test runs to automatically detect and log issues before they reach production. Results can be kept informational, giving your team early visibility without creating GxP record obligations, or promoted to support formal qualification decisions when needed.
When application changes break test cases, the system detects the break, analyses what changed, and proposes a targeted fix including before/after evidence. AI assistance also covers test design, generation, and ongoing maintenance. In a GxP context, all AI-generated proposals require SME review and approval before any change is applied to a validated test asset.
We support regulated life sciences teams, including QA, validation, and IT stakeholders, who face increasing change, frequent releases, and high-volume test execution and documentation demands.
Release timelines are being pushed and product quality is at risk due to outdated validation test execution and documentation practices.
Change keeps scaling, but validation cannot scale manually.
We combine regulated delivery expertise with trusted automation engineering and platforms to accelerate validation testing & documentation in life sciences.
Business partner of Pharma Management Consulting. Global automation and digital transformation leader delivering AI-powered intelligent automation solutions as a service.
Gold partner of Valenta. 7-time Gartner Magic Quadrant Leader in RPA. The industry leading platform for building software robots that automate repetitive tasks, integrate systems, and scale enterprise workflows.
UiPath joining Veeva's AI Partner Program is a strong signal that life sciences is moving toward purpose-built, compliant automation. Pairing agentic AI with RPA can cut manual testing, speed up releases, and give more time back to people.
UiPath being named a Leader in Gartner's Magic Quadrant for AI-Augmented Software Testing Tools is a strong signal that agentic testing is going mainstream. For life sciences, the value is clear: less manual testing effort, faster release cycles, and happier people.
When working with regulated life sciences teams on IT system implementation and maintenance, I keep running into the same problem: testing and validation are often manual, slow, and resource-heavy, and they become a bottleneck for delivery. I believe there's a better way.
Pharma Management Consulting was founded in 2023, to support life science companies with project management, agile delivery, compliance, and validation. In 2025, Pharma Management Consulting became a business partner of Valenta, a global leader in intelligent automation and digital transformation. Working closely with managing Director Sven De Groodt, we aim to help life science organizations modernize software testing and validation through AI-powered automation, delivered as a service.
I've delivered projects for organizations across the sector, including Novo Nordisk, NNIT, Novartis, Orphazyme, Oncopeptides, Ascendis Pharma, Zealand Pharma, Santen Pharmaceutical, Elos Medtech, Epista Life Science, and Emerson Process Management.
Based in Copenhagen, Pharma Management Consulting helps life science companies transform the way they test and validate regulated software.
Let's explore how we can remove the validation bottleneck in your operations. Tell us a bit about your situation and we'll get back to you within one business day.
Thank you for reaching out. We'll get back to you within one business day.