we offer
Test Documentation and Reporting
Medtech and Pharma are documentation-heavy industries, and poorly produced documentation can lead to failing regulatory approval or delays in the development process.
Our specialists follow good documentation practices (e.g. ALCOA+ principles) that ensure traceability, accountability and trustworthiness in test documentation and reporting. We are thorough and professional, which results in unambiguous documentation that is readable and usable for years to come.