Patient Registries

Coram Clinical Trials can help you gain essential knowledge about drug use and treatment outcomes in real-world clinical practice by working with you to establish patient registries and/or observational studies. We will work with you to design and implement the ideal study to:

• Meet market challenges successfully
• Address FDA safety commitments
• Collect the data you need to demonstrate your drug's true therapeutic value

Observational Studies

We have successfully managed studies in all major therapeutic areas, and can help you design and manage non-interventional clinical research programs.

These programs include:

• Disease or patient registries
• Post-approval product registries
• Post-approval safety surveillance studies
• Research-based physician education programs