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Indiko™ Plus Clinical Chemistry System

Thermo Fisher Scientific

Experience an uncompromised level of performance and ease of use with the Thermo Scientific™ Indiko™ Plus Clinical and Specialty Chemistry analyzer. This fully-automated random access benchtop system for clinical and specialty chemistry testing, combined with system reagents and consumables form a fully-supported, complete system solution offering confidence to daily work.

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HybridSPE®-Plus Plates

Merck

Our HybridSPE ® -PLus plates effectively remove phospholipids and proteins from biological matrices in a simple pass-through method for accurate and reproducible LC-MS analysis. Unlike other phospholipid removal SPE products on the market, the unique retention mechanism of HybridSPE ® allows for separation of even very hydrophobic analytes from phospholipid contaminants.     

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MAS PAR TDM Controls

Thermo Fisher Scientific

Check therapeutic drug monitoring test procedures with ready-to-use, liquid assayed multi-analyte Thermo Scientific™ MAS™ PAR™ TDM Controls, therapeutic drug controls with assayed values designed for therapeutic drugs and common immunoassayed test procedures on most automated instruments. Liquid, ready to use Features three significant levels Includes values for major automated analyzers

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Supel™ Swift HLB SPE Cartridges

Merck

Supel™ Swift HLB is a polymeric stationary phase for solid phase extraction (SPE) prior to instrumental analysis. It has both hydrophilic and lipophilic functional groups for the extraction of a broad range of compounds from aqueous samples. It retains analytes having diff erent polarities and Log P values due to its hydrophilic and lipophilic balance (HLB) property.

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RX 50 Bio Chemistry Analyzer

Micro Lab Instruments

SALIENT FEATURES User-friendly software End Point Method - Storage of Abs of Reagent blank in memory. Editing of patient iD, Name (12 characters), Factor Print out of laboratory name & Doctor's name. For Kinetic test: Online Graph & OD. Graph editing facility. Estimation of the result. Battery Back-up for 90 mins - Optional Air purge between samples. Coagulation test like PT with parameters ISI value / INR /…

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Breath Biopsy® Services

Owlstone Medical

Combining high resolution accurate mass mass spectrometry and world-leading breath analysis expertise to offer complete breath biomarker discovery and validation solutions. Breath Biopsy Services provide versatile Breath Biopsy sample analysis and reporting driven by GC-Orbitrap technology and supported by a rigorous quality assurance process ensuring reliable, high sensitivity VOC biomarker detection.

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Respiratory VOC Panel

Owlstone Medical

A targeted panel of compounds with established relevance for respiratory diseases enabling high confidence, non-invasive disease detection and monitoring. Each compound is supported by evidence from breath research studies of relevant respiratory diseases and disease processes. The panel is available as an aspect of Breath Biopsy Services and panels for other disease applications are in development.

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rTest COVID-19/Flu qPCR Diagnostic Kit

MultiplexDX, Inc.

Main features At least one-month room temperature stability Improved sensitivity of proprietary RdRP and E assays  Multiplexed version  With RNase P assay as an internal control SARS-CoV-2 full genomic RNA spiked with human RNA used as a positive control 100% clinical accuracy Ultrasensitive limit of detection of 2 RNA copies/rxn for all targets (SARS-CoV-2, IAV and IBV) 100% specific for SARS-CoV-2, and WH…

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EP06, Evaluation of Linearity of Quantitative Measurement Procedures

Clinical and Laboratory Standards Institute

This document provides both manufacturers and users of quantitative measurement procedures with an economical and user-friendly method of validating and verifying the linearity interval. EP06 can also be used to determine the extent to which a quantitative measurement procedure meets medical requirements or the manufacturer’s linearity interval claims.

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EP06, Evaluation of Linearity of Quantitative Measurement Procedures

Clinical and Laboratory Standards Institute

This document provides both manufacturers and users of quantitative measurement procedures with an economical and user-friendly method of validating and verifying the linearity interval. EP06 can also be used to determine the extent to which a quantitative measurement procedure meets medical requirements or the manufacturer’s linearity interval claims.

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