Pharmaceutical GCP Compliance Auditing Services (GCP Clinical Trials)

Good Clinical Practice (GCP) typically falls under the auspices of a Clinical Quality System. Clinical Quality Systems address compliance in its entirety: from protocol development to site management and GCP audits, and clinical study reports. In essence, the stronger your Clinical Quality System, the more likely your study will be compliant and able to progress to the next submission phase expeditiously.

Companies that are bound by regulations for clinical studies, manufacturing of pharmaceutical products or medical devices, production of raw materials, or laboratory services, require routine inspection and GxP audits. The companies are expected to be compliant and continuously improving. GCP Compliance Auditing Services suppliers maintain alignment with new, existing, and changing regulations and industry standards that evolve throughout the drug product and device lifecycle.