NeuMoDx Molecular
Developer of automated, sample-to-result molecular diagnostic platforms integrating robotic liquid handling, unitized microfluidic cartridges, onboard nucleic acid extraction, stabilized dry reagents and real‑time PCR detection to support continuous random‑access, high‑throughput laboratory workflows.
Industries
Nr. of Employees
small (1-50)
Patents
Products
Mid‑throughput automated molecular system
Mid‑sized automated instrument that performs automated nucleic acid extraction, amplification and multi‑channel fluorescence detection for clinical laboratories (sample‑to‑result).
High‑throughput automated molecular system
High‑capacity automated system scaled for large‑volume diagnostic laboratories with continuous random‑access and full automation from sample load to result.
Liquid lysis reagent for automated extraction
Packaged liquid lysis reagent formulated for use in automated nucleic acid extraction workflows and cartridge systems.
NeuMoDx™ 96 Molecular System
Designed for automated extraction and isolation of nucleic acids, as well as automated amplification and detection of target nucleic acid sequences by fluorescence-based PCR. Intended for IVD use in performing validated nucleic acid testing in clinical laboratories.
NeuMoDx™ 288 Molecular System
Designed for high-volume clinical laboratories requiring automated extraction, isolation, amplification and detection of target nucleic acid sequences by fluorescence-based PCR. The 288 scales to match the demands of large-throughput diagnostic environments.
NeuMoDx Molecular Diagnostic Automation Platform
An integrated sample-to-answer molecular diagnostic system that combines nucleic acid extraction and PCR amplification in a single closed-system workflow, enabling walkaway operation and continuous random-access processing for rapid and reliable molecular testing.
Mid‑throughput automated molecular system
Mid‑sized automated instrument that performs automated nucleic acid extraction, amplification and multi‑channel fluorescence detection for clinical laboratories (sample‑to‑result).
High‑throughput automated molecular system
High‑capacity automated system scaled for large‑volume diagnostic laboratories with continuous random‑access and full automation from sample load to result.
Liquid lysis reagent for automated extraction
Packaged liquid lysis reagent formulated for use in automated nucleic acid extraction workflows and cartridge systems.
NeuMoDx™ 96 Molecular System
Designed for automated extraction and isolation of nucleic acids, as well as automated amplification and detection of target nucleic acid sequences by fluorescence-based PCR. Intended for IVD use in performing validated nucleic acid testing in clinical laboratories.
NeuMoDx™ 288 Molecular System
Designed for high-volume clinical laboratories requiring automated extraction, isolation, amplification and detection of target nucleic acid sequences by fluorescence-based PCR. The 288 scales to match the demands of large-throughput diagnostic environments.
NeuMoDx Molecular Diagnostic Automation Platform
An integrated sample-to-answer molecular diagnostic system that combines nucleic acid extraction and PCR amplification in a single closed-system workflow, enabling walkaway operation and continuous random-access processing for rapid and reliable molecular testing.
Services
On‑site installation and hands‑on operator training to integrate systems into laboratory workflows.
Telephone and email support, service contracts and prioritized technical assistance for deployed instruments.
Provision of room‑temperature stable reagents and single‑use microfluidic cartridges optimized for automated workflows.
Supply of general‑purpose reagents and consumables, plus documentation to support laboratory‑developed tests and user‑validated assays on the platform.
On‑site installation and hands‑on operator training to integrate systems into laboratory workflows.
Telephone and email support, service contracts and prioritized technical assistance for deployed instruments.
Provision of room‑temperature stable reagents and single‑use microfluidic cartridges optimized for automated workflows.
Supply of general‑purpose reagents and consumables, plus documentation to support laboratory‑developed tests and user‑validated assays on the platform.
Expertise Areas
- Automated molecular diagnostic workflows (sample‑to‑result)
- Microfluidic cartridge design and scale manufacturing
- Real‑time quantitative PCR and multiplex assay development
- Nucleic acid extraction chemistry and inhibitor removal
Key Technologies
- Real‑time quantitative PCR (qPCR)
- Unitized microfluidic cartridges
- Magnetic bead‑based nucleic acid extraction
- Lyophilized / dry reagent stabilization
News & Updates
Participation in molecular diagnostics conferences with live system demonstrations and workflow presentations.
Article on how laboratory automation addresses workforce shortages, turnaround time pressures, manual errors and increasing test volumes; discusses total laboratory automation and molecular sample‑to‑answer systems.
Overview of dry reagent stabilization approaches, cold‑chain challenges, operational impact of ambient‑stable reagents and stability validation requirements.
Technical review of microfluidic technologies, unitized cartridges, autonomous lanes and manufacturing considerations for cartridge‑based diagnostics.
Discussion of clinical applications and requirements for quantitative viral load assays across HIV, HBV, HCV and transplant monitoring.
Overview of extraction methods, specimen‑specific challenges, automation advantages, RNA stability concerns and design criteria for robust clinical extraction workflows.
Participation in molecular diagnostics conferences with live system demonstrations and workflow presentations.
Article on how laboratory automation addresses workforce shortages, turnaround time pressures, manual errors and increasing test volumes; discusses total laboratory automation and molecular sample‑to‑answer systems.
Overview of dry reagent stabilization approaches, cold‑chain challenges, operational impact of ambient‑stable reagents and stability validation requirements.
Technical review of microfluidic technologies, unitized cartridges, autonomous lanes and manufacturing considerations for cartridge‑based diagnostics.
Discussion of clinical applications and requirements for quantitative viral load assays across HIV, HBV, HCV and transplant monitoring.
Overview of extraction methods, specimen‑specific challenges, automation advantages, RNA stability concerns and design criteria for robust clinical extraction workflows.