Interventional Trials

We excel in providing comprehensive services for interventional trials, ensuring efficiency and compliance throughout the process. Our expertise begins with studying feasibility, and evaluating the viability and potential success of a clinical trial. We assist in site evaluation and selection, identifying optimal locations to conduct trials based on various factors such as patient population and regulatory environment.

Our services extend to planning, budgeting, and resourcing, where we help clients develop a detailed plan that aligns with their objectives and resources. We manage trial master files (TMF) to ensure all documentation is maintained accurately and securely. Veram also handles submissions to Institutional Review Boards (IRBs) and Regulatory Authorities, ensuring all protocols are followed and approvals are obtained. With our cloud-based Electronic Data Capture (EDC) solutions, we facilitate trial initiation, patient recruitment and retention, trial monitoring, and project management. Safety reporting and archival of essential documents are also managed meticulously to ensure compliance and success in interventional trials.