We support your sites throughout the study to ensure protocol adherence, patient safety, and data integrity.
We conduct monitoring visits from site selection to close-out, ensuring high-quality data and regulatory compliance.
We identify, document, and support the resolution of site-level issues to keep your trial on track.
We support your sites throughout the study to ensure protocol adherence, patient safety, and data integrity.
We conduct monitoring visits from site selection to close-out, ensuring high-quality data and regulatory compliance.
We identify, document, and support the resolution of site-level issues to keep your trial on track.
Clinical Monitoring is a core service that ensures the integrity, quality, and regulatory compliance of your study.
Our experienced Clinical Research Associates (CRAs) serve as the main contact persons for the study sites, overseeing study conduct from site selection to close-out. Our CRAs verify data accuracy and protocol compliance through on-site visits and remote site management activities, while acting as trusted partners to support sites in successfully completing the study.
Our Clinical Monitoring team ensures seamless site initiation, ongoing support, and efficient site close-out. With strong communication and coordination, we build trusted partnerships with investigators and site staff to foster compliance and data quality throughout the study.
We conduct risk-based on-site and remote monitoring guided by ICH-GCP and sponsor requirements. Our CRAs verify data accuracy, subject safety, and protocol adherence, identifying issues early to prevent deviations and ensure inspection readiness at all times.
At GCPS, Clinical Monitoring means more than compliance checks, it’s proactive problem-solving. Our CRAs collaborate closely with sites to resolve operational challenges, prevent delays, and keep your study on track for timely and successful delivery.
Clinical Monitoring is a core service that ensures the integrity, quality, and regulatory compliance of your study.
Our experienced Clinical Research Associates (CRAs) serve as the main contact persons for the study sites, overseeing study conduct from site selection to close-out. Our CRAs verify data accuracy and protocol compliance through on-site visits and remote site management activities, while acting as trusted partners to support sites in successfully completing the study.
Our Clinical Monitoring team ensures seamless site initiation, ongoing support, and efficient site close-out. With strong communication and coordination, we build trusted partnerships with investigators and site staff to foster compliance and data quality throughout the study.
We conduct risk-based on-site and remote monitoring guided by ICH-GCP and sponsor requirements. Our CRAs verify data accuracy, subject safety, and protocol adherence, identifying issues early to prevent deviations and ensure inspection readiness at all times.
At GCPS, Clinical Monitoring means more than compliance checks, it’s proactive problem-solving. Our CRAs collaborate closely with sites to resolve operational challenges, prevent delays, and keep your study on track for timely and successful delivery.
Our CRAs have successfully finished over 100 trials in all phases and more than 40 indications.
Our team of 20+ in-house CRAs can cover 10+ countries directly. With the help of our partner CROs, we are able to monitor even large worldwide studies.
Our CRAs have 200+ years of combined clinical research experience.
