Computerized systems are the basis of clinical trials, Quality assurance, and pharmacovigilance in the contemporary life sciences and regulated industries. By providing end-to-end Computer System Validation (CSV) validation services that are audit-ready, risk-based, and compliant with international regulatory standards, we assist organizations in achieving and preserving compliance.
Having expertise of more than 15 years in pharmacovigilance industry, we have helped many clients validating their dynamic systems, guaranteeing data integrity, patient safety, and product quality all the way through the system life cycle.
System type that we support:
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