Triligent International is a contract research organization (CRO) that specializes in pre-clinical and clinical research in most therapeutic areas for the pharmaceutical, biotechnology and device industries. Services include: GCP, GMP, GLP audits and consulting; Part 11 audits and consulting; system validation; Phase I, Phase II, Phase III and Phase IV monitoring; project management; and clinical development. All services provided are in compliance with FDA, US 21 CFR (Code of Federal Regulations) and International Conference on Harmonisation (ICH) laws, rules, regulations and guidelines.