Clinical Studies Monitoring
The monitoring services offered by JDP in clinical studies include site initiation visits, site monitoring visits, remote monitoring, close-out visits, site management and regulatory submissions.
To guarantee the caliber and integrity of your clinical trials, JDP provides a variety of clinical study monitoring services. Our team of certified and skilled clinical research associates (CRAs) can monitor the advancement of your clinical trials and confirm that the protocol, standard operating procedures (SOPs), good clinical practice (GCP), and relevant laws and regulations are followed in their conduct, recording, and reporting. We gather, organize, and analyze clinical data from a variety of sources, including electronic case report forms (eCRFs), electronic data capture (EDC), and clinical trial management systems (CTMS), using cutting-edge technology and processes.
Our range of monitoring services is tailored to meet the specific requirements and goals of your research project. We are capable of carrying out centralized, remote, on-site, or a mix of these types of monitoring. We can also adjust the frequency and plan of our monitoring to the degree of complexity and danger involved in your research.
Our global network of CRAs is capable of covering numerous nations and areas. We are capable of managing clinical studies for a range of indications and therapeutic areas. Additionally, we have access to local resources and expertise, including contacts at the site, law enforcement, and ethical committees.
We make certain that the protocol, SOPs, GCP, and other pertinent standards are followed by the sites we have chosen. In addition, we keep an eye on the participants’ safety and wellbeing and notify the relevant parties of any unfavorable occurrences or deviations. To ensure the completeness and correctness of the clinical data and documentation, we regularly audit and review the records.