Webinars and Sponsored Roundtables — Register Now

Tuesday, July 21, 2026, 11:00-11:30 AM CT

Learning Objectives:
  • 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

Bio-Rad Laboratories Clinical Diagnostics Group

PR4100 Microplate Reader

Company

Bio-Rad Laboratories Clinical Diagnostics Group

Name of instrument

PR4100 Microplate Reader

Contact

Maria Crisostomo   

Email

maria_crisostomo@bio-rad.com

City, State

Hercules, CA

Phone

800-224-6723   

Website

http://www.bio-rad.com

Type of instrument

immunoassay

List price/First year sold in U.S.

—/2012

Targeted hospital bed size/Targeted test volume

Company manufactures instrument

yes

Other models in this family of analyzers

No. of units in clinical use in U.S./Outside U.S. (countries)

Dimensions (H × W × D)/Instrument footprint

5.3 × 13.7 × 7.4 in./—

Weight empty/Weight fully loaded

5.7 lbs./—

No. of different measured assays onboard simultaneously

No. of user-definable (open chemistry) channels

Test throughput per hour/Assay run time

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 Ion-selective electrode basic metabolic panel

Stat time until completion/specimen throughput for Ion-selective electrode complete metabolic panel

Typical time delay from ordering stat test until aspiration of sample

Fully automated microplate immunoassay system

no

Methodologies supported

enzyme immunoassay

Separation methodologies

none necessary

Stat time until completion of a ß-hCG test

Stat time until completion of a cTn test

• Typical time delay from test order to aspiration of sample

Reagents refrigerated onboard/Reagents ready to use

no/—

Reagent lot tracking/Reagent inventory

no/no

Reagent form/Reagents barcoded

liquid chemistry (open reagent system)/—

Separate reagent pack for each specimen/for each test run

Walkaway capability/Walkaway duration

no/—

Design of sample-handling system

batch, benchtop

Uses washable cuvettes/Uses disposable cuvettes

no/no

Min.–max. sample volume that can be aspirated at one time 

Min. reaction volume/Min. specimen volume/Min. dead volume

Dedicated pediatric sample cup

no

Primary tube sampling

no

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

no (microplate reader)/no (microplate reader)

Pierces caps on primary tubes

no

Protects against probe collision

no

Detects clots/liquid level/short sample

yes/yes/no

Detection or quantitation for hemolysis, icterus, lipemia, clots

hemolysis, icterus, lipemia, clots not available

Dilutes patient samples onboard/Susceptibility to carryover

no/—

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)/no

Typical calibration frequency for ISE/therapeutic drugs/drugs of abuse/general chemistries/immunoassays

Automatic programmable start/Automatic programmable shutdown

no/no

Onboard real-time QC/Onboard software capability to review QC

no/no

Supports multiple QC lot numbers per analyte

no

Waste management

manually by user

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, Codabar, Code 39, Code 128)/no

Lab can control analyzer from remote computer

no

Instrument can diagnose its own malfunctions

no (operator intervention required to order parts)

System malfunctions can be diagnosed via remote monitoring

no

UPS backup power supply

no

Data-management capability/LIS or EHR systems interfaced

no/—

LIS interface provided/Bidirectional interface capability

no/no

Modem servicing provided/Service engineer on-site response time

no/—

Mean time between failures

Average scheduled maintenance time by lab personnel

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 training slots)/1 day (at customer site)

Advanced operator training/Extra charge for follow-up or advanced training

no/yes

Warranty provided/Cost of annual service contract (24 h/7 d)

yes/—

Distinguishing features (supplied by company)

comprehensive data-analysis software for full traceability; LIS connectivity; compact size–space saver

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