Regulatory and Clinical Technology
Cost-Effective Innovation Across the Drug Development Lifecycle
New technology innovations make it possible for your entire company – and its partners – to work with a single source of truth for data that is extended throughout the lifecycle. By moving steadily toward digitalization and a new generation of unified, integrated solutions, regulatory and clinical organizations can evolve to truly take advantage of the changes occurring in the industry. PAREXEL is at the forefront of this evolution - and is helping to drive the shift. As one of the world’s leading biopharmaceutical services providers and the only one offering complete end-to-end technology solutions back by 35 years of clinical services expertise, PAREXEL is uniquely positioned to support our clients in making this transition.
The Perceptive Cloud represents the technology alliance between PAREXEL and Microsoft. Perceptive Cloud, built on Microsoft Azure, combines the power and intelligent capabilities of cloud computing, global regulatory compliance and top tier security with PAREXEL’s industry expertise and technology solutions. This truly breakthrough convergent platform streamlines workflows for a seamless user experience with persona-based access, while improving transparency and enabling advanced insights to drive better decisions, faster.
Perceptive MyTrials® Analytics provides a suite of mobile-enabled dashboards designed to leverage the power of cross-study metrics presented in new and meaningful ways. This single-entry point gives access to data analytics for all your studies simultaneously, in real-time, providing actionable information within sight of the people who can use it to benefit your company’s current and future performance.
Our Data-Driven Monitoring solution helps you leverage data to assess risk and direct monitoring activities, manage data quality and workload assignments at any given site. It uses data visualization and analytics tools to measure key risk indicators and trigger interventions using sophisticated risk-assessment methodologies, and provides remote/centralized monitoring to manage sites and clinical data interrogations.
IMPACT® CTMS ensures that all clinical research across the globe will be speaking in the same language, using the same terms, tracking in similar ways. This allows a common view company-wide, but with a great deal of local flexibility when the need arises. Whether your organization is a biotech start-up or a global pharmaceutical company, IMPACT CTMS can integrate multiple sources of information involved in the clinical trial process, providing a single source of truth throughout the entire lifecycle.
DataLabs® EDC has a proven track record of helping organizations improve valuable resources, gain efficiencies and maintain quality data. It includes targeted source document verification and robust safety monitoring to help streamline the entire process, starting from study design all the way to collection, management and reporting of clinical trial data. Delivered through the Perceptive Cloud, DataLabs EDC is integrated with PAREXEL’s clinical technology ecosystem to help users plan, design and conduct clinical trial programs in a single place.
LIQUENT InSight® is the leading end-to-end, integrated Regulatory Information Management (RIM) platform available in the market today. Its publishing solutions offer comprehensive and powerful tools to enable the rapid creation, review and submission of regulatory dossiers. This is a single solution for document tracking and approval, supporting the entire life span of documents and products and helping to enable compliance, including submission planning, publishing, archival and registration management.