Non-Interventional Trials

Our specialty is in ensuring the success of each study. Our approach begins with thorough study feasibility assessments, helping clients identify the most suitable sites and investigators for their research. We assist in site evaluation and selection, ensuring that the chosen sites meet all necessary criteria for conducting the trial effectively.

Our team is skilled in managing the entire process, from the preparation of files and contract negotiation to submissions to Ethics Committees and Regulatory Authorities. We provide support in setting up and maintaining study files, ensuring that all documentation is complete and compliant with regulatory standards. Veram Bioclinical Solutions also offers expert safety reporting services, ensuring that all adverse events are reported accurately and in a timely manner. Our commitment to excellence extends to the completion of studies as per agreed budgets and timelines, ensuring that clients can trust us to deliver results efficiently and effectively.