Pharma, Diagnostic and MedTech 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.
