Regulatory Affairs| Clinical Trials| Pharmacovigilance

Clinical Trials

Savante Consulting Limited will project-manage Phase III and IV clinical trials and Bridging studies to support Marketing Authorization Applications and achieve other desired outcomes for the client. We are able to get approvals for trials from Regulatory bodies, including National Regulatory Agencies and Hospital Ethics Committee, select sites, appoint investigators recruit patients, provide logistics for managing data and trial materials. We generate final documentation for final submission to the regulatory agencies.