ethica CRO is a specialized Contract Research Organization (CRO) focused on medical aesthetics, dermatology, and neurology, supporting pharmaceutical, biotechnology, and medical device companies operating in highly regulated environments.

We provide end-to-end support for the design, management, and execution of clinical trials conducted in accordance with FDA, Health Canada, and EMA regulatory requirements. Our teams work closely with sponsors seeking a highly specialized, agile, and governance-driven CRO, rather than a volume-based provider.

A defining element of ethica CRO’s operating model is the full integration of a Human Research Protection Program (HRPP) across all clinical and operational activities. By structurally placing the research participant at the center of study design, governance, and execution, we strengthen data integrity, regulatory credibility, and long-term study value.

ethica CRO is the only CRO worldwide to have received three independent HRPP accreditations, reflecting a mature and consistently applied framework for participant protection, research ethics, and governance.

Core expertise:

●	Medical aesthetics clinical trials

●	Clinical trial design and execution

●	Regulatory compliance (FDA, EMA, Health Canada)

●	Research governance and audit readiness

●	Human Research Protection Program (HRPP)

Partner with a specialized CRO

If you are developing products in medical aesthetics, dermatology, or neurology and are looking for a specialized, governance-driven CRO, learn more about our capabilities and regulatory approach.


ethica CRO

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ethica CRO

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