Clinical Trial Management System
CRO functions with a centrally based management system. Our researcher and research associate’s posses tremendous experience and has marked their niche in the clinical Research industry. We have best of resources and expertise for the process management of all ongoing Clinical Researches and Clinical Trials. Our Researchers and Clinical trial project management team works in line altogether for effective results of the study. At CRO, all the personnel involved in research are trained in the regulatory guidelines (such as GCP-ICH, CFR, GMP, GLP etc.) so that they can have better understanding of ethics and legal restrictions before proceeding further in the study. In addition we also regularly keep quality monitors to see that no gap remains in quality and research of any study.
Broadly our management systems see following 3 aspects to be systematically coordinated
Strategic Planning
This is the first phase in which management research upon feasibility, scope and plan development. It manages the review of the previous literature in study field. As these aspects get cleared, management tracks down issues and concerns that may arise in the course of Clinical Research/Trial Study.
Trial Management
Trial management is the central aspect for all the I-IV phases of Clinical Researches. Here, in the trial management service, CRO does complete monitoring activities of I-IV phase of clinical trials. CTM team indulges in inventory management, site management, proper documentation of reports and SOPs, QC visits, Site Training, enabling the resources etc
Recruitment Management
CRO handles all type of recruitments related to Clinical Researches. Here it’s the work of management team to fulfill the entire requirement for Clinical Researches on time. They facilitate the requirements and ensure that every resource exhibit their potential to the maximum. The recruitments can be of diversified nature
- Researchers Recruitment
- Patient Randomization
- Volunteers & Drug availability
