Quality Assurance

At inVentiv Health Clinical the Quality Assurance (QA) team interacts directly with clients to understand the specific requirements for their product development project. Our quality and regulatory affairs specialists ensure adherence to these client requirements and any applicable regulations from the U.S. Food and Drug Administration (FDA), Canada’s Health Products and Food Branch Inspectorate, European Union, ANVISA and other international agencies during each phase of the clinical trial process. Our experience and oversight means that our clinical and bioanalytical services comply with Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and International Conference on Harmonisation (ICH) GCP guidelines (E6). Quality is integrated into all of our processes.

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