Continuous monitoring of global regulatory changes and guidance relevant to pharmacovigilance and drug safety.
Assessment of regulatory changes for their impact on your PV system, processes, and compliance obligations.
Support for the implementation of new or revised regulatory requirements into your PV operations and documentation.
Updating of internal policies, SOPs, and training materials to reflect the latest regulatory expectations.
Preparation of tailored regulatory intelligence reports to keep your teams informed and audit-ready.
Training and awareness programs for your teams on new and emerging regulatory requirements in PV.
Coverage of regulatory intelligence for both global and local markets, ensuring comprehensive compliance.
Ongoing support for continuous improvement of your PV system in response to regulatory intelligence findings.