Freedom EVO 100/150 Liquid Handling Workstation by TECAN
| Brand | TECAN |
|---|---|
| Origin | Shanghai, China |
| Model | Freedom EVO 100 / Freedom EVO 150 |
| Deck Positions | 20 / 28 (excluding optional expansion modules) |
| Pipetting Range | 0.5–1000 µL |
| Dimensions | Model-dependent |
Overview
The Freedom EVO 100/150 Liquid Handling Workstation is a modular, benchtop automation platform engineered for precision liquid handling in biobanking, clinical research, and high-throughput assay development laboratories. Built on TECAN’s proven EVO architecture, it employs air displacement pipetting with integrated CO-RE (Combinatorial REservation) technology to support multi-channel, low-volume transfers with high reproducibility. The system operates under programmable protocols that enforce consistent aspiration/dispense kinetics, temperature-controlled deck environments (optional), and real-time liquid level sensing—enabling reliable processing of diverse biological matrices including whole blood, plasma, serum, saliva, and cryopreserved cell suspensions. Designed for integration into ISO 15189-accredited biobanking workflows and GLP-compliant sample management pipelines, the Freedom EVO platform supports traceability-critical operations through audit-ready execution logs and hardware-level event timestamping.
Key Features
- Modular deck architecture with 20 or 28 standardized SBS-format positions—scalable via optional expansion modules for storage, incubation, or detection peripherals
- High-precision air-displacement pipetting with dual-range channels (0.5–10 µL and 5–1000 µL) using disposable or fixed tips, calibrated per ISO 8655
- Integrated liquid level detection and clog sensing across all pipetting channels, minimizing failed transfers and enabling adaptive protocol recovery
- TECAN FluentControl™ software with drag-and-drop workflow builder, parameterized method templates, and version-controlled protocol libraries
- Optional on-deck temperature control (4–40 °C) for reagent stabilization and cold-chain integrity during long-run biobank processing
- Robust mechanical design compliant with IEC 61000-6-2 (EMC immunity) and IEC 61000-6-3 (EMC emission) standards for shared laboratory environments
Sample Compatibility & Compliance
The Freedom EVO 100/150 accommodates standard microplate formats (96-, 384-, and 1536-well), tube racks (including 1.5 mL and 2.0 mL conical tubes), and custom labware via user-defined coordinate mapping. It handles viscous, foaming, and volatile samples—including glycerol-diluted DNA stocks, DMSO-containing compound libraries, and protein-rich lysates—through adjustable aspiration speed, surface tension compensation, and post-aspiration delay settings. For biobanking applications, the system meets core requirements of ISO 20387:2018 (Biobanking—General requirements for biobank operations) and supports implementation of chain-of-custody records aligned with GDPR and HIPAA data governance frameworks. All instrument-generated metadata—including pipette calibration certificates, tip lot traceability, and run logs—are exportable in CSV or XML format for regulatory submission.
Software & Data Management
FluentControl™ provides full lifecycle method development, execution, and validation support. It includes built-in electronic lab notebook (ELN) integration, role-based user access control (with password policies and session timeouts), and configurable audit trails compliant with FDA 21 CFR Part 11 requirements—including electronic signatures, immutable log entries, and change history tracking. Data export adheres to MIAME and MIAPE reporting guidelines where applicable. Instrument diagnostics, firmware updates, and remote monitoring are accessible via secure HTTPS interface with TLS 1.2 encryption. System backups and archive retention policies can be scheduled and validated independently of operational runtime.
Applications
- Automated biobank inventory management: primary tube aliquoting, plate-to-plate normalization, barcode-driven sample routing
- Genomic workflow preparation: PCR setup, NGS library normalization, qPCR master mix dispensing
- Clinical trial sample processing: EDTA-plasma fractionation, PBMC cryovial labeling, stability study timepoint transfers
- QC/QA testing: reference material dilution series, inter-laboratory proficiency panel distribution, calibration curve generation
- Compound management: small-molecule stock solution serial dilution, dose-response plate formatting, solubility screening
FAQ
Is the Freedom EVO 100/150 compatible with third-party labware and consumables?
Yes—via FluentControl™’s Labware Definition Editor, users can import or manually configure dimensions and coordinate offsets for non-TECAN plates, tubes, and reservoirs.
What calibration documentation is provided with the system?
Each unit ships with factory-issued ISO/IEC 17025-accredited calibration reports for pipetting accuracy and precision at defined volumes (1, 10, 100, and 1000 µL), traceable to NIST standards.
Can the system operate unattended overnight?
Yes—the platform supports scheduled start/stop, power-fail recovery, and automatic tip waste ejection; continuous operation requires ambient temperature control and uninterrupted power supply (UPS) integration.
Does TECAN provide validation support for GxP environments?
TECAN offers IQ/OQ documentation packages, risk assessments (per ISO 14971), and qualified vendor support for PQ execution in regulated biobanking and pharmaceutical labs.
How is software update management handled?
Updates are delivered via TECAN’s secure Software Update Portal; each release includes versioned release notes, impact analysis, and rollback procedures validated per internal quality system requirements.
