Webinars and Sponsored Roundtables — Register Now
Tuesday, July 21, 2026, 11:00-11:30 AM CT
- Explain how transparency and manufacturer partnerships improve quality, consistency, and decision-making confidence in specimen management.
- Evaluate blood collection tubes beyond cost and commodity assumptions, incorporating clinical impact and risk into decision-making.
- Assess the potential risk points when using a blood collection device that has not been cleared for a specific purpose.
Roundtable presenters Nick Fingland, PhD, PMP, Senior Director, R&D Operations and Science, BD, and Chris Farnsworth, PhD, D(ABCC), Section Head of Clinical Chemistry, Professor of Pathology and Immunology, Washington University School of Medicine.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Wednesday, July 29, 2026, 1:00-2:00 PM ET
Learn about digital pathology technology that is future-ready, yet practical for today’s
laboratory needs.
Webinar presenters Scott Hammond, Senior Systems Consultant, Digital Pathology Division, Wexner Medical Center, Department of Pathology, and Ursula Hofer, Imaging Technologist, Pathology Digital Imaging Lab, Wexner Medical Center, Department of Pathology, and Sandra Banky, PA(ASCP), Director of Operations, Wexner Medical Center, Department of Pathology.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Subspecialties
Interactive Product Guides
Product Spotlight
Tosoh Bioscience
| Company | Tosoh Bioscience |
|---|---|
| Name of instrument | AIA-360 |
| City, State | Grove City, OH |
| Phone | 800-248-6764 |
| Website | |
| Type of instrument | immunoassay |
| Operational type/Model type | continuous random access/benchtop |
| List price/First year sold in U.S. | —/2004 |
| Targeted hospital bed size/Targeted test volume | —/monthly: < 500 |
| Company manufactures instrument | yes |
| Other models in this family of analyzers | AIA-900, AIA-2000 |
| No. of units in clinical use in U.S./Outside U.S. (countries) | ~600/> 7,000 (worldwide) |
| Dimensions (H × W × D)/Instrument footprint | 21 × 16 × 16 in./2.1 sq. ft. |
| Weight empty/Weight fully loaded | 61 lbs./— |
| No. of different measured assays onboard simultaneously | 25 (25 can be run and calibrated at one time) |
| No. of user-definable (open chemistry) channels | — |
| Test throughput per hour/Assay run time | 36/20 min. |
| No. of direct ion-selective electrode channels | — |
| Detection methods | — |
| Stat time until completion/specimen throughput for ion-selective electrode | — |
| Stat time until completion/specimen throughput for basic metabolic panel | — |
| Stat time until completion/specimen throughput for complete metabolic panel | — |
| Typical time delay from ordering stat test until aspiration of sample | — |
| Fully automated microplate immunoassay system | — |
| Methodologies supported | fluorescence enzyme immunoassay (FEIA) |
| Separation methodologies | — |
| Stat time until completion of a ß-hCG test | 20 min. |
| Stat time until completion of a cTn test | 20 min. |
| • Typical time delay from test order to aspiration of sample | — |
| Approximate No. of tests per reagent set/Reagent type | 100 (20 tests per tray)/unit dose test cup |
| Reagents refrigerated onboard/Reagents ready to use | no/yes |
| Reagent lot tracking/Reagent inventory | yes/no |
| Reagent form/Reagents barcoded | dry chemistry (closed reagent system)/yes |
| Separate reagent pack for each specimen/for each test run | yes/— |
| Walkaway capability/Walkaway duration | yes/58 min. or 25 specimens or 25 tests/assays |
| Design of sample-handling system | carousel |
| Uses washable cuvettes/Uses disposable cuvettes | no/no |
| Min.–max. sample volume that can be aspirated at one time | 10–100 µL |
| Min. reaction volume/Min. specimen volume/Min. dead volume | 10 µL/110 µL/100 µL |
| Dedicated pediatric sample cup | no |
| Primary tube sampling | yes |
| Accommodates most standard tube sizes/Accepts nonstandard tube sizes | yes/— |
| Pierces caps on primary tubes | no |
| Protects against probe collision | — |
| Detects clots/liquid level/short sample | yes/yes/yes |
| Detection or quantitation for hemolysis, icterus, lipemia, clots | — |
| Dilutes patient samples onboard/Susceptibility to carryover | no/none |
| Automatic rerun capability | no |
| Sample volume can be diluted to rerun out-of-linear-range high results | no |
| Sample volume can be concentrated to rerun out-of-linear-range low results | no |
| Autocalibration/Multipoint calibration supported | no (calibrants are not stored onboard)/yes |
| Typical calibration frequency for ISE/therapeutic drugs/drugs of abuse/general chemistries/immunoassays | —/—/—/—/90 days most assays |
| Automatic programmable start/Automatic programmable shutdown | no (5 min. start-up time)/no |
| Onboard real-time QC/Onboard software capability to review QC | no/no |
| Supports multiple QC lot numbers per analyte | — |
| Waste management | automated collection onboard instrument |
| Sample barcode-reading capability/Autodiscrimination | yes (Interleaved 2 of 5, Codabar, Code 39, Code 128)/yes |
| Lab can control analyzer from remote computer | no |
| Instrument can diagnose its own malfunctions | no |
| System malfunctions can be diagnosed via remote monitoring | — |
| UPS backup power supply | yes |
| Data-management capability/LIS or EHR systems interfaced | Tosoh 501RP+/— |
| LIS interface provided/Bidirectional interface capability | no/no |
| Modem servicing provided/Service engineer on-site response time | — |
| Mean time between failures | 888 days (displays error codes for troubleshooting) |
| Average scheduled maintenance time by lab personnel | daily: 5 min. |
| Maintenance records kept onboard for user/vendor | no/no |
| Maintenance training demonstration module onboard | no |
| Training included with purchase/Avg. time for basic user training | yes/2 days (at customer site) |
| Advanced operator training/Extra charge for follow-up or advanced training | — |
| Warranty provided/Cost of annual service contract (24 h/7 d) | yes (1 year)/— |
| Distinguishing features (supplied by company) | unit dose test cup; dry reagent, no premixing or reagent preparation; immunoassay method free from biotin interference; compact size, broad menu with fast results; 90-day calibration stability for most assays |