Learn how PAREXEL Informatics develops the technological innovations to make the process of drug development faster, more accurate, more productive and easier to track.
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Perceptive MyTrials® Platform and Infrastructure
Our converged suite of applications is underpinned by our powerful platform of enabling technologies and framework standards, ensuring our combination of products and components interoperate seamlessly and cohesively.
Platform technologies include:
• Clinical Technologies Integration Platform (CTIP), delivered using industry-standard integration and Extract Transform Load (ETL) software.
• Enterprise portal software, to provide the framework through which to surface our applications, data and information.
• Enterprise reporting application, to provide high-quality and feature rich reporting solutions for all performance metrics reports and detailed application data reporting.
• Identity management software, governing the identity and access of all our users for all our hosted applications, and enabling our single sign on capability.
Using Perceptive MyTrials provides the ability to leverage the full power of our enabling platform. SaaS customers benefit from our ability to simply consolidate and report performance data from across our hosted product suite.
The suite is greater than the sum of its parts. Learn why we are driven by
the need to make life easier for those conducting clinical trials. Read more.
Study Management and Monitoring
PAREXEL Informatics offers an impressive, sustainable track record of successfully applying and managing medical imaging in clinical trials. We are known for our medical, technology and regulatory expertise as well as our emphasis on imaging compliance and validation - key areas that require knowledge and expertise.
Regulatory Information Management
Regulatory Information Management (RIM) is defined as the effective and efficient collection, storage, retrieval and communication of regulatory information. RIM processes include defining product authorization targets, managing regulatory submission plans, creating and gathering submission information, producing and submitting the submission output and managing the product registration.
Clinical Data Management
The DataLabs® EDC (Electronic Data Capture) solution is uniquely focused on simplifying workflows and delivering superior user experiences. Its advanced EDC features help streamline the entire process starting from study design all the way to collection, management and reporting of clinical trial data.
Randomization and Trial Supply Management
PAREXEL® Informatics provides automated randomization and supplies management through its ClinPhone® RTSM (Randomization and Trial Supply Management) solution. Our services are offered by the industry's most experience and trusted provider of IVR (Interactive Voice Response) and IWR (Interactive Web Response) technologies.
Electronic Clinical Outcome Assessments (eCOA)
Clinical Outcome Assessments (COAs) measure a patient’s symptoms, overall mental state, or the effects of a disease or condition on how the patient functions. COAs can be used to determine whether or not a drug has been demonstrated to provide treatment benefit. COA types include ePRO (electronic Patient Reported Outcomes).