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Clinical Studies


The CRO Group offers a robust suite of Clinical Trial Services to support the needs of medical device developers as well as other trial sponsors from premarket submissions to post-marketing advertising campaigns, and virtually everything in-between.

All of our Clinical Trial Services comply with Internationally Harmonised Good Clinical Practices (ICH-GCPs) required by FDA under 21 CFR 812, the European Directives and recognised if not required for approval in virtually all corners of the Globe.

Our Clinical Trial Service menu starts with study designs resulting in plans and protocols with endpoints, methodology, and statistical considerations that fit your budget and business goals.