ABOUT CES

Clinical Encapsulated Services, (CES) was founded in 1996 as a pharmaceutical manufacturer of encapsulated clinical supplies for pharmaceutical drug studies. We are an FDA cGMP facility registered with the New York State Board of Pharmacy.

We are thankful to our clients for their continued patronage and are proud to be associated with all of them. From the biggest and most nationally renowned institutions and successful companies to the equally appreciated start-up company or small institution, we are grateful to all who utilize our services.

OUR
HISTORY

We began this journey back in 1996 by working with the Cleveland Clinic Foundation, National Institute of Health (NIH) and Pfizer in regards to the African American Study of Kidney Disorder and Hyper-tension, a large multi-arm, multi-year and nationwide study. CES was the drug manufacturer contracted by the Cleveland Clinic to perform the over-encapsulation of the drug product to secure the blind for the study.

Over the past twenty-five years we have continued to service not only the Cleveland Clinic but those in need of supplies for their clinical trials. We are happy to handle orders of all sizes and have manufactured batches from as few as 300 capsules to batch sizes of 1,000,000 capsules.

The company remains solely a manufacturer of capsule products, specializing in the over-encapsulation of tablets and capsules as well as the matching placebo for: clinical trials, drug studies, and R&D and test batches. However, CES’ encapsulation processes are not limited to manufacturing products for clinical studies; in addition to performing clinical manufacturing we apply the same strict, quality guidelines and GMPs to the manufacturing of dietary supplements and assorted nutriceuticals. CES was applying GMP drug manufacturing procedures to the production of supplements and nutritionals since 1997, long before the FDA came out with the current dietary manufacturing guidelines.