Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.
As requirements for clinical trial disclosure and transparency continue to increase, IQVIA can help you meet critical submission dates with services ranging from consultancy, clinical trial registration, results postings and redactions, to clinical report anonymization and plain language summaries.
Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.
Partner with compliance experts to create, implement and manage efficient, end-to-end processes that ensure your organization is compliant with global engagement and transparency regulations and codes.
Harness the power of global human expertise combined with automation, artificial intelligence (AI) and machine learning (ML) to design, build and execute end-to-end safety solutions.
Manage trial master files from planning through archive with solutions designed to improve workflow efficiency, promote collaboration, and support compliance.