Electronic data capture and reporting Start your eClinical journey with an EDC for collecting, processing, and reporting trial data. Easily set up studies on your own — no training required. Get visibility into study health with dynamic dashboards. Add more virtual elements as your trial needs...
This includes onsite inspection ofdocumentation that demonstrates the validation of software which has been developed in-house for clinical data reporting.Andrea BakerGlaxoSmithKline
Software for clinical trials comes in many forms. It can be tailored to a specific task or it can be comprehensive in its applications across the entire process. Essentially, it’s one or more pieces of software used by CROs, biotech, and pharma companies to aid in the design, running, a...
BSI Life Sciences offers a complete, integrated, and easy to use modern CTMS with eTMF functionality—and a lot more. See our services and request a demo today.
Design and Analysis of clinical trials involves evaluating several designs, simulating them to assess performanceand proceeding with one chosen design, collecting and analyzing trial data, carrying out adaptations as permitted by the protocol, and reporting trial results. Each of these specialized ...
The CancerGrid approach to clinical trials information systems is based on a metamodel developed from the CON-SORT statement of best practice in reporting randomised controlled trials. The metamodel is instantiated with meta-data elements drawn from a repository, to create a model of a particular ...
JMP Clinical has the potential to, frankly, do anything needed for conducting and reporting clinical trials, whether it is central statistical monitoring, signal detection, narrative creation, building clinical data warehouses or, indeed, full-blown clinical trial reporting with close to a single push...
AllTrial.Netcalls for “all past and present clinical trials to be registered and their full methods and summary results reported” — a beneficial registry to counterbalance the bias of only reporting positive results. Negative results, while not as “interesting” to publish, are results — and...
Microsoft Clinical Trial Initiation solution Finally – there are other organizations and software vendors that are thinking along these lines. Check out the following solutions: A solution in place in the US Department of Veteran Affairs TENALEA– Trans European Network for Clinical Trials Services ...
How can custom software help with regulatory compliance in clinical trials? In particular, custom software can incorporate features to comply with regulatory requirements (tracking, labeling, licenses, etc.), automate the gathering of compliance data, and provide tools for documentation and reporting. ...