Alcedis Plugins are modular extensions designed to enhance the Alcedis eCRF platform with readily available functionalities for the most common and critical clinical trial processes. Developed based on best practices, these plugins simplify documentation, streamline workflows, and ensure compliance across all phases of clinical research. They cover a wide range of operational needs including data validation, patient safety, randomization, reporting, and multilingual support.

Features

• Real-Time Data Validation: Smart automation reduces up to 80% of manual data cleaning. Patient data is easily monitored via modern interfaces for CRAs, data managers, and project managers.
• Role-Based Access & Audit Trails: Ensures full transparency and secure data handling.
• Codepicker: Fast and accurate coding of adverse events, medical histories, and medications using MedDRA, WHO-DD, NCI, ICD, OPS, ICD-O-3.
• Randomization: Automated patient randomization upon registry.
• Tumor Assessment: Standardized assessments based on RECIST criteria.
• Patient Reported Outcomes: Over 50 licensed questionnaires and surveys for electronic use.
• eMARS: Electronic medication diary for tracking oral medication intake.
• Translator: Direct translation of free-text entries within the eCRF.
• Language Switcher: Supports multiple languages including English, French, Spanish, Italian, Chinese, Russian, and more.
• User-Adaptive Dashboards: Oversight of site activities, recruitment, documentation completeness, milestones.
• Elastic Semantic Search: Quickly find answers to key questions.
• In-App Bookmarking: Keep relevant information visible at all times.
• Forecasting & Alerts: Ensure studies stay on track.
• Pharmacovigilance Tools: Confidently manage safety processes in compliance with regulations.
• Remuneration: Transparent and secure payment processing for investigators and participants.
• Organizer: Schedule visits, set reminders, and manage calendars.
• Data Management: Handle queries and monitor data cleaning activities.
• eFeasibility: Manage site identification, performance analysis, and contracting.
• Alcedis Academy: Training and certification for study users, with optional re-training and documentation.
• eConsent: Capture digital patient signatures on iOS/Android devices, compliant with data protection laws.
• Drug Accountability & Sample Tracking: Monitor lab kit storage, sample shipment, and drug accountability.
• Monitoring Tool: Organize visits, generate reports, track protocol violations and follow-ups.
• Support Chat: Interactive online support within the eCRF.
• Laboratory Templates: Create lab templates with range checks for various markers.
• CRF Status: Visual traffic-light system for form status.
• Standard Reports: Built-in reports for multiple processes.
• Report Designer: Custom reports in CSV, XLS formats via intuitive interface.
• eSignature: Electronic signing of case report forms with status tracking.

Benefits

• Comprehensive Functionality: Covers all critical clinical trial processes.
• Efficiency: Reduces setup time and manual work.
• Transparency & Oversight: Dashboards, audit trails, and reporting tools ensure full control.
• Compliance: Meets regulatory standards for safety and data protection.
• Flexibility: Modular design allows tailored platform expansion.
• User Empowerment: Training tools and multilingual support enhance usability.
• Cost-Effective: Maximizes operational efficiency and reduces overhead.