ethica CRO is a full-service Contract Research Organization (CRO) that conducts and manages ethical clinical research on behalf of sponsors within the international pharmaceutical, biotechnology, medical device, nutraceutical, and cosmeceutical industries.
We offer end-to-end clinical research communications services in compliance to the highest scientific and ethical standards.
Our experienced and highly-qualified clinical project managers ensure that your study objectives and timelines are met. Study-specific applications help you track and manage study metrics anytime, anywhere.
Our clinical monitoring is conducted in accordance with a well-designed monitoring plan, ICH-GCP Guidelines, applicable regulatory requirements, and our accredited participant-centered procedures.
Our team of experts will help you translate numbers into ideas, concepts, and regulatory approvals. Through our proven data quality and integrity procedures, we produce credible and reliable data that you and the public can trust.
Whether the study design is parallel, factorial, cross-over, sequential, Bayesian, superior or non-inferior, our team will use the latest and most appropriate statistical tools and techniques to maximize your data’s clarity and potential.
We can add value and scientific knowledge throughout your product life-cycle by providing strategic and logistical support for Medical Affairs related research including proof-of-concept studies, Investigator-initiated-trials, meta-analyses, etc.
Whether the study design is parallel, factorial, cross-over, sequential, Bayesian, superior or non-inferior, our team will use the latest and most appropriate statistical tools and techniques to maximize your data’s clarity and potential.
We can add value and scientific knowledge throughout your product life-cycle by providing strategic and logistical support for Medical Affairs related research including proof-of-concept studies, Investigator-initiated-trials, meta-analyses, etc.
