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Contract Research Organizations (CROs)


Contract Research Organizations (CROs) specialize on a specific phase of the pharmaceutical value chain. Ensuring that laboratory research or clinical trials remain compliant solicits constant efforts to maintain a proper quality management system, perform validation or qualification.


Clarmon’s solutions enable contract research companies to reduce the amount of effort and time required to manage regulatory documents and tasks. Companies can move securely from manual and paper based documentation to an electronic environment that automates routine tasks.


Users without deep GxP knowledge can create consistent documents and maintain them up-to-date with less effort. The simple web and word based interface ensures that documents are always controlled and can be managed from any location.


Configurable GxP workflows supported by automatic audit trails accelerate collaboration and ensure compliance.
QAvalid enables fully electronic validation, supporting test execution, results capture and recording of test evidence.


The total time of validation is reduced through built in requirements management features, instant traceability matrix and instant change impact, reuse of information or automatically generated and linked documents.



Clarmon’s solutions help CROs:




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