We help life science companies automate software test execution and documentation
We help life science companies automate software testing and documentation, so validation experts can focus on judgment and oversight, not manual testing and compiling documentation.
Orchestrate validation test runs with automated environment preparation, data setup, and run sequencing.
Test evidence is generated automatically and compiled into validation documents using rule-based logic.
Experts manage exceptions and review and approve outcomes. Decisions stay with experts.
Schedule continuous test runs during off-hours to continuously verify that critical systems and processes are working.
We support regulated life sciences teams validating GxP and non-GxP IT systems where frequent change and high-volume testing create a significant validation workload.
Release timelines are being pushed and product quality is at risk due to outdate software test execution and documentation practices.
"Change keeps scaling, but validation throughput cannot scale manually."
Since I began working with regulated teams in the pharmaceutical industry in 2018, I've noticed a reoccuring challenge: people spend far too much time and effort manually testing and validating IT systems.
I founded Pharma Management Consulting in 2023 to offer my expertise in project management, compliance, and validation. In 2025, I partnered with Valenta to bring specialized validation automation solutions to the life science industry.
I have delivered projects for companies such as Novo Nordisk, NNIT, Novartis, Orphazyme, Oncopeptides, Ascendis Pharma, Zealand Pharma, Santen Pharmaceutical, Elos Medtech, Epista Life Science, and Emerson Process Management.
Pharma Management Consulting is based in Copenhagen and its main objevtive is to help life science companies in the Nordic region transform their testing and validation process.
Let's explore how we can remove the validation bottleneck in your operations.