GXP Audits are an international ethical and scientific quality standard for the design, conduct, performance, monitoring, auditing, recording, analyses & reporting of clinical trials.

Quality and Compliance is a system for ensuring that products are consistently produced and controlled according to quality standards.

Pharmacovigilance (PV) is responsible for monitoring the safety of medicines in normal clinical use and during clinical trials.

Regulatory affairs ensures in managing the approval and compliance of pharmaceutical products throughout their market lifecycle.