Clinical Trial Support
IMS provides a full range of services to support biomedical research ideas from inception through implementation and into publication. The IMS team approach provides flexibility and rapid deployment for full study management or for specific tasks.
Clinical trials and biomedical research projects are diverse. Our staff has successfully supported numerous project types. Examples are:
- Clinical trials - pharmaceutical, device, and vaccine
- Early disease detection projects
- Health survey processing
- Epidemiological data collections
IMS biomedical research staff and statisticians work closely with investigators and site staff to develop study protocols, manuals and data collection instruments. Assistance in regulatory compliance is provided. Our biomedical editors review and code clinical and other research data. They interact with site research staff frequently to confirm patient eligibility, provide randomized treatment assignments and answer questions on protocol procedures. They ensure data of the highest quality through query and error resolution. IMS staff may travel to the research centers to provide training or to monitor study progress.
IMS provides assistance in data analysis and preparation of data displays for publication. We collaborate with manuscript authors in the writing and submission of papers. IMS staff have co-authored hundreds of scientific publications.
IMS provides a broad range of services for our clients, including but not limited to: Data Coordinating Centers; Clinical Trials support; Data hosting and Analysis; Application Development; Website implementation and hosting; Software As A Service (SaaS); and others.
Choose one of our services below to learn more about what we offer at IMS: