OCKHAM
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Quality Statement
Ockham will ensure that all clinical trials are performed to the highest standards, in compliance with applicable U.S. Food and Drug Administration (FDA) and International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) regulations and guidelines. The Senior Management Team is committed to continuous improvement, defining and reviewing quality objectives on a regular basis. Internal process improvements are managed concurrently with clinical trial projects. Continuous training and testing ensures that clinical research personnel are up to date with all professionally required knowledge. Quality objectives are always part of each individual’s performance evaluation.