Ensuring the safety of clinical trial subjects is one of the main responsibilities of the study, sponsor, and institutional review boards, where the primary goal is to protect the life and health of clinical trial subjects.
X7 Research offers safety monitoring services at any stage of clinical trials, including the post-marketing stage in Russia, EAEU, CIS, EU.
MANAGEMENT OF ADVERSE EVENTS
SAFETY DATABASE MAINTENANCE
PREPARATION OF ANNUAL SAFETY RE-PORTS
X7 Research has been involved in safety in clinical trials since 2010. The key points of our specialists’ work are to ensure full control of adverse events, including distant ones, and fulfillment of all legal requirements.