GCP guidelines set forth by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) provide a framework to ensure the ethical conduct, safety, and quality of clinical trials. Audit and monitoring are essential components of GCP compliance and play a vital role in the success of clinical studies.
Zenovel's GCP audit and monitoring services empower clinical trials with compliance checks, data accuracy, and early risk identification for successful research
Zenovel provide affordable, innovative, and high-quality solutions to pharma industry with ethics driven research and increasing accessibility to high quality medicine worldwide