Depending on your requirements, from bringing in novel cannabinoid-related compounds or conducting late-phase clinical studies, we will be able to provide a turn-key solution for your needs.
MCRC provides fully trained Clinical Research Associates with a wealth of pharmaceutical experience and clinical trial knowledge across all phases of clinical trials to ensure that monitoring is conducted to the highest standard.
All trials are monitored in accordance with regulatory requirements and ICH GCP. To ensure the seamless exchange of information each clinical research trial is assigned a Clinical Trial Manager as a single point of contact.
MCRC has an extensive number of Standard operating procedures to conduct clinical trial research activities. Additionally, MCRC can adapt seamlessly to your SOP and requirements if desired.