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PAREXEL® provides leading solutions to integrate systems and processes to help companies simplify the concurrent use of multiple technologies involved in clinical trials. PAREXEL’s integrations are delivered by our dedicated eClinical Technology Services (eCTS) experts who have an in-depth understanding of advanced technologies, clinical development processes and validated system integrations.
Underpinning PAREXEL's integration solutions and services is our cutting-edge Clinical Technology Integration Platform (CTIP). Built on proven middleware, it is a unique environment designed to facilitate seamless two-way exchange of data across different systems via reliable and repeatable integrations. For optimal scalability and convenience, we also offer validated connectors with built-in integration functionalities for clients requiring ready-made integration solutions to be installed alongside the enterprise implementations of our products.
PAREXEL'S proven integration solutions and services enable your key systems to possess consistent and accurate data, enhancing your ability to make timely and informed decisions. By eliminating the need for re-keying data and duplication of activities across multiple applications, biopharmaceutical companies can dramatically simplify user workflow and allow diverse clinical trial applications to work together synergistically.
• Integration with DataLabs® EDC, ClinPhone® RTSM, IMPACT® CTMS, Medical Imaging and ePRO as well as other third-party solutions
• Real-time data interchange making data instantly available across multiple systems
• Elimination of data reconciliation and duplicate activities
• Ability to share consistent trial data across the entire enterprise
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.
Electronic Data Capture
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).