many services
one goal
Quality assurance
InnoPharma has always pursued full and accurate compliance with Good Clinical Practices (GCP), to safeguard the rights of human participants and to protect the integrity and validity of clinical data of each trial or investigation managed.
Designed programs
Tailored approacH
InnoPharma provides the systems approach required to ensure compliance with ICH/GCP consolidated guidelines. Our audit experience includes a wide range of therapeutic areas and all development phases.
InnoPharma is equally adept at auditing clinical programs managed by InnoPharma, or stand-alone programs managed by clients or other CROs.
Quality’s the best policy
Don’t hesitate to ask Innopharma’s professionals for a thorough audit of your systems, testing facilities and documents/reports to ensure adherence to GCP.
For each audit, they’ll work with you to develop a client-specific audit plan to address in detail each performed task. At the conclusion of each audit, InnoPharma prepares a written report, including detailed observations and a corrective action plan, if required.