Latest solutions, case studies, interviews, practical articles for clinical trials operations, data management, technology, investigative sites and services.
The sponsor-site relationship is an essential consideration in investigative sites' willingness to participate in clinical trials and sites' ability to perform successfully. To better understand factors that impact this relationship, the Tufts Center for the Study of Drug Development, in conjunction with...
Moreover, in a recent poll, 57% of respondents indicated that sites need to improve clinical trial productivity because of low profitability, whereas 29% suggested that everyone else is realizing efficiencies, so they need to do it as well [3].IT systems and EHR adoption is im...
The survey Impact Assessment of eClinical Technologies and Industry Initiatives on Sites commissioned by Oracle Health Sciences and conducted by the Society for Clinical Research Sites (SCRS) reveals a downward trend in site satisfaction with the current eClinical environment when participating in clinica...
SPECIAL FEATURE: Paediatric Clinical Trials: An Investigative Site PerspectiveBefore selecting the patient population, key elements of the protocol should be weighed against the specific paediatric population of interest, as not allpaediatric subpopulations are createdequal. For example, determinatio...
Since 1994, CenterWatch, has been the recognized global leader in providing clinical trials information to a broad and influential spectrum of clinical research professionals ranging from sponsors and CROs, to investigative sites, technology solut...
Many forms of bias can occur within trials, and how these have been dealt with need to be clearly reported. The JIDSP endorses the Consolidated Standards of Reporting Trial (CONSORT) Statement and requires authors to report their clinical trials fully according to the latest revision ...
Preto CL. Pressures at the front lines: investigative sites and contract research organizations in Canadian clinical trials. PhD Dissertation. University of British Columbia; 2014. https://circle.ubc.ca/handle/2429/45810 . Accessed 13 Nov 2014....
The impact of the structure and organization of clinical research services (data management model) on the workload of clinical research coordinators (CRCs) at investigative sites is undocumented. This paper describes three types of data management models and their potential influence on the workload ...
Explores the ethical and scientific criteria for clinical research standards governing innovative organizational practices at investigative sites in the U.S. Collaboration with clinical research sponsors; Overview of the sponsor-inve...