P21 is a unified cloud suite to streamline the design, build, and submission of clinical trial data, as well as ensure the quality, integrity, and compliance of your data. Learn more about Pinnacle 21 Certara Integral Repository Certara Integral™ is a single, validated, 21 CFR Part 11 com...
By harnessing the power of AI and ML, researchers can accelerate drug discovery, enhance patient selection criteria, optimize trial design, and ensure real-time monitoring and safety. Octalsoft Integrates advanced AI/ML capabilities into our our comprehensive suite of eClinical software solutions to ...
Providing design, simulation and execution of adaptive trials across all phases of development Providing advice and guidance on the logistical and operational requirements for successful adaptive trial execution Overseeing ongoing adaptive trials to ensure that trial integrity and validity are maintained at ...
it’s one or more pieces of software used by CROs, biotech, and pharma companies to aid in the design, running, and reporting of trials at any stage of the trial lifecycle.
Trial Design Partnering Clinical Tech Regulatory Patient Recruitment DCTs Find A Partner Events STREAM Clinical Trial Software and Services PartnersThe conduct of a clinical trial requires numerous software and technology tools to make the trial process more efficient. These include a clinical trials ...
AiCure is the world’s first patient engagement AI. Better adherence, data quality, and patient outcomes start here.
Clinical trial design is a key aspect of the successful conduct of clinical trials. It involves deciding parameters such as the number of patients, the length of the trial, the comparator arm (in the case of randomized controlled trials) using information on current treatments, the anticipated ef...
Umbrella trial design guided by molecular phenotypes of a certain disease Due to shared genetic alterations across different cancer types, the basket trial design was developed with the core theme of “treating different diseases with the same treatment”. In contrast, the umbrella trial design was ...
There are two main documents compiled during trial design - protocols and case report forms (CRFs). Aprotocoldescribes the objective, methodology, evaluation criteria, and even trial location. It’s compiled by a group of experts, and in the US, EU, and Japan, a clinical trial protocol shou...
Clinical Operations departments are responsible for the design, development, and review of clinical trial protocols, monitoring and tracking the execution of clinical trials, and ensuring the compliance of clinical sites with trial protocols. TrackWise by Sparta Systems offers a Clinical Operations ...