Automation simplifies your work

Automation can help you meet the challenges of increasing test volumes and staff shortages. 

Your solution should have:

• Automated quality control features to drive reproducibility and standardization
• A fully integrated sample preparation and cell analysis system for a complete walk-away solution

Consistently reproducible

To have confidence in your results, you must trust your workflow. These workflows must be consistently reproducible to streamline your lab and allow you more time to focus on complex cases. 

Standardization and result integrity requires:

• End-to-end traceability of specimens and reagents
• Automation of sample preparation, acquisition, and analysis
• Automation of reagent cocktails
• Connectivity with your Laboratory Information Systems for seamless results transfer

The power of standardization

Standard operating procedures help labs stay organized, collaborative, and efficient. 

Automation helps you standardize across your staff, your workflows, and other sites.

• Standardization through automation reduces manual errors and ensures the reproducibility of quality data.
• Assay transferability ensures you are standardized across instruments and to other sites.
• Standardized and validated protocols make training new staff effortless.

Increase sample throughput and efficiency

Staff shortages are impacting labs and are predicted to get worse. Solutions that are efficient allow your staff to fully walk away and provide efficiency advantages that create a sustainable lab for years to come.

Keep your lab running smoothly with:

• A complete walk-away solution—reduces manual steps that may lead to errors requiring repeat testing, result reporting delays, and work injuries from repetitive tasks such as pipetting
• Continuous loading capabilities to help increase your throughput

Flexible and modular

Recall your current testing environment, but realize you need to evolve and grow. Flexibility in the solution is key to ensuring you have the ability to offer new clinical applications.

Your solution should be flexible:

• In allowing for the use of different vendor reagent vials and specimen tubes and bulk solutions 
• By allowing you to build your own flexible workflows for any custom application
  
• Due to Clinical and Laboratory Standards Institute (CLSI) 21CFR Part 11 compliance

Complete traceability with audit trail

You should always know why results look a particular way. For that, you need to trust your staff and your solution to deliver consistent results. And when things change, you need to have a complete traceability log to determine exactly why. 

Your automated solution should have:

• Traceability of specimens, reagents, and worklists along the all—process journey
• In Vitro Diagnostic (IVD) certification 

IVD instrumentation with end-to-end traceability automates reporting, which facilitates ISO 15189 accreditation.