With our experience in hard-to-reach indications, a global network of clinical research professionals, and regulatory know-how, the Raremark team engages patients in clinical research, improves the informed consent process, and accelerates recruitment; on budget, on time – every time.
We help to give clinical studies an identity, essential in competitive therapeutic areas
Our online recruitment tactics increase referral rates through previously untapped patient populations, saving time and money
Through our global network and localised print materials, we provide tailored support to clinical trial sites
Our engaging eConsent materials help guide patients and caregivers through the complex process of informed consent
For more information on how Raremark can support your clinical trial, please contact our Client Services Director, Peter Coë. Email: firstname.lastname@example.org