ethica is the first CRO in the world to be accredited for its Human Research Protection Program. The clinical research projects we manage hold up to the highest standards of ethical and clinical practices.
ethica CRO is well versed in all applicable international, American, and Canadian laws, regulations, and guidelines. You can rest assured that all research activities managed by ethica CRO are consistently compliant.
Human Research Protection Program (HRPP)
ethica CRO’s accredited HRPP is at the core of its mission. Our responsibility extends to a review, education, surveillance and engagement process that includes employees, investigators, vendors, and partners of the organization.
ethica CRO’s business continuity plan, HRPP, accredited SOPs and highly trained professionals are your assurance to maintaining clinical research activities and safeguarding data during a disruptive event.
Quality Management System (QMS)
ethica CRO’s QMS framework is comprised of five interconnected elements in support of compliance, safety, continuous improvement, and a quality-driven culture, for the benefit of human research participants, sponsors, and sites.
Get in touch
Have any questions about our clinical research quality standards or want to submit a request for proposal from our CRO? Get in touch via our contact page we will get back to you as soon as possible.