Expert Provision of Responsible Persons and Qualified Pharmacovigilance Personnel (QPPV)
At Soterius, we offer expert support by providing highly qualified Responsible Persons for Clinical Trials and Qualified Persons for Pharmacovigilance (QPPV), ensuring rigorous oversight and regulatory compliance throughout the clinical development process. Our experienced professionals act as essential points of contact, managing safety reporting obligations, overseeing clinical safety management, and ensuring your trials align with global regulatory requirements.
Local Safety Officers and Safety Representatives for Global Coverage
Our global network of Local Safety Officers and Local Safety Representatives provides tailored, regional expertise essential for navigating diverse regulatory landscapes. With deep knowledge of country-specific safety reporting requirements and pharmacovigilance obligations, our local experts facilitate smooth communication with regulatory authorities and investigators, enabling consistent and compliant safety management across all trial locations.
