Achiever LIMS for Clinical Research provides full traceability of trial, sample and patient data combined with a low-code, configurable Laboratory Execution System (LES) so you can manage different study protocols and workflows.
Achiever LIMS for Clinical Research securely centralises and standardises your clinical research data and workflows to improve data quality, increase process efficiency and meet regulatory compliance.
Offering a unique combination of LIMS and CRM functionality, Achiever LIMS for Clinical Research can be configured to meet diverse and complex process and data requirements using its low-code, no-code configuration tools and Laboratory Execution System (LES).
The LIMS’ Laboratory Execution System (LES) guides researchers step-by-step through your SOPs and processes to ensure consistency, reproducibility, and compliance. The low code, no code, configurable LES enables you to design and adapt workflows to meet your unique study protocols as well as your lab processes and needs.
Flexible, configurable workflows to manage sample receipt and dispatches enables you to trace all sample movements between internal and external labs. In addition, the comprehensive events audit trail and record versioning capabilities provide complete traceability across all data and activities.
Comprehensive CRM features support supplier and customer management activities as well as participant recruitment. Plus, automated communications and alerts send personalised emails, SMS and notifications to both internal and external recipients in accordance with GDPR.
Connecting to your lab instruments, scanners, and systems, the LIMS reduces data transcription errors, as well as increasing productivity by removing unnecessary administration.
