Remarque
An end-to-end clinical trial platform
Remarque is designed to simplify study management and propel innovation.
Overview
Clinical development is increasingly complex. Patient and sites are broadly dispersed. Use of decentralized approaches is expanding. Studies include an average of 8 vendors, many collecting essential data. This environment can lead to process discrepancies and siloed work, making it difficult to predict and assess risk. Failing to manage risk is a leading cause of trial delays.
Our Solution: All Your Data in One Platform
Remarque improves performance by simplifying study planning, execution, and close out in one platform, bridging Premier Research’s clinical and therapeutic expertise with robust data insights.
Organizations around the world use Remarque for better clinical trial insights.
- More than 15 million data points processed daily
- Over 300 studies run including, 200+ using a risk-based approach
- More than 1.3 million startup activities tracked
- Greater than 50,000 monitoring visits documented and filed
| The Solution | The Result |
|---|---|
| Consolidated Data. Seamlessly merges data from disparate systems into a single location. | We employ a scalable, source agnostic data aggregation process to work with your existing technology systems to centralize data for full visibility in one place. |
| Identified Risk. Quickly identify risks to drive greater collaboration and inform decision making. | Real-time analytics and machine learning deliver effective risk prediction, detection, and analysis so system insights can guide strategic decision-making. |
| Informed Action: Use analytics and AI-powered reports to create data-driven action plans. | Analytics and AI-powered reports, and comprehensive, role-based data views drive action by supporting effective communication and task management. |
Capabilities
Design and Project Management: Bring together your scientific design, country, and enrollment plan to accurately forecast and track your study timeline, risk assessment, resource needs, and costs.
Study Startup: Accelerate feasibility, site, and country startup with centralized libraries of vendors, contacts, investigators, and sites.
Integration Hub: Hundreds of integrations available across all types of study vendors bring your data together seamlessly.
Operational Analytics: Track performance through effective KPIs and make informed decisions with out-of-the-box and readily accessible dashboards, visualizations, and reports.
Clinical Analytics: Leverage your centralized clinical data and our library of pre-built visuals and reports to make key decisions around studying safety, quality, and progress.
Documentation: Consolidate all your documentation needs, action plans, and timelines to reduce inefficiencies, limit document transfers, and improve auditing.
Monitoring and Risk Management: Centralize all your monitoring needs – onsite, remote, medical, safety, risk–based quality management (RBQM) – by putting your data in one place to rapidly identify and respond to risks.
AI Insights: Leveraging Large Language, NLP (Natural Language Processing) and other advanced models to improve your decision making and reduce complex manual review.
Closeout – Track closeout activities and ensure data readiness for analysis and submission.
Integrations
Optimize with a science-driven, patient-centered approach to clinical research
A customized approach drawing on medical expertise
Integrated, technology-enabled approach to drive efficiency and quality across clinical development
Quality and clarity from
an exceptional team of regulatory medical writing experts
Ensure safety through all stages of clinical development
Therapeutic, product development, and regulatory experience help streamline the path to approval
Industry leaders with comprehensive submission experience position your product strategically
A more efficient, cost-effective path from development to commercialization
resources
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Ready to get started? So are we.
Drop us a line to learn more about how we can help.