Clinical Trial Services

Unlike other GXP disciplines, GCP clinical research is performed at many different institutions and frequently on a global basis. Each investigator site is different and has its unique set of problems, yet the data from this research must be comparable and gathered in a consistent way that meets the letter and spirit of GCP regulations and guidelines to be viable in regulatory submissions.

Service Offering	Examples
Interphase Systems can help you: Address and correct issues pertaining to computerized systems used to create, modify, maintain, archive, retrieve, or transmit clinical data intended for submission to the FDA, Training Clinical Trial monitors, Documentation development and, Audits	GCP Training of Clinical Monitors, Medical Monitors and investigational site teams Standard Operating Procedure development Development of Clinical Trials Documentation See Audits for additional Clinical Trial support