Rapid Extraction System (RES) from CambTEK
5 Feb 2013
Extracting a solid dose form into a liquid dose form is currently a very slow and manual process. Watch this video to learn about the Rapid Extraction System from CambTEK, which has been designed to simplify sample preparation, freeing analysts from inaccurate and laborious processes, and reducing significant bottlenecks within laboratory and manufacturing workflows. Learn about the key features and application areas of this innovative system.
About the company
CambTEK
Located within the innovative Cambridge technology circle, the highly skilled CambTEK team is developing automated laboratory solutions, specializing in sample preparation.
The CambTEK Rapid Extraction System (RES) enables increased productivity in many food and life-science industries, including pharmaceutical, agrochemical and veterinary.
CambTEK has developed a sample preparation instrument for rapid extraction of solid dose forms and gels.
This Rapid Extraction System (RES) delivers a step-change in performance when compared to the existing methods, and is achieved using robust technologies and an intelligent consumable. The CambTEK RES delivers many advantages, including:
Reduced analysis time
Improved quality control
Increased analyst productivity
Increased laboratory throughput
High reproducibility
In-Process data
Reduction in solvent consumption, with improved methods
Reduced cost per test* and rapid ROI
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Rapid Extraction System (RES)
CambTEKThe CambTEK Rapid Extraction System – A new approach to automated sample preparation of solid dosage forms for improved quality of data and productivity. CambTEK's Rapid Extraction System (RES) delivers a step-change in performance compared with the existing methods, and is achieved using robust technologies and an intelligent consumable. Utilizing non-invasive turbulent flow with the option of ultasonics the RES delivers many advantages, including: Reduced Sample Preparation touch time Improved QC/QA Increased laboratory throughput In-process data Easily prepare beads, capsules, gels, intermediate granulations, pellets, powders, solid & semi-solid matrices, stents, suppositories, swabs, and tablets (both normal and prolonged release) Reduction in solvent consumption, with improved methods Intuitive User interface and control for both skilled and non-skilled operators Barcode sample tracking and chain of custody Reduced cost per test, with improved methods Application areas include: content uniformity testing, blend uniformity testing, stability analysis, tablet assay testing, capsule assay testing, drug assay testing, other impurities testing, quality analysis, batch release testing, and quality by design, dose content uniformity, batch release, stability assay, shelf life (end of life) testing, dose or drug content, drug impurities assay, bulk assay, incoming QC of raw materials, QC end product assay, pat assays or testing, at-line testing, in-process control assay test (IPCS), production QC, blend assay, blend homogeneity test, bulk drug purity assay, excipient compatibility tests, design space assays, experimental design for design space, process qualification (PQ) batches, process validation batches (PV), cleaning validation samples, occupational hygiene samples (people drug exposure monitoring – on filters), complaint samples or returns from market, design verification, incoming QC of raw materials, end product testing of solid products, compliant samples, spot testing by food inspectors.Industry sectors include: pharmaceutical R&D and production, veterinary, food, fine chemicals, and forensics.