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This whitepaper demonstrates the High Performance Liquid Chromatography (HPLC) separation and analysis technique and highlights the importance of using water of sufficient purity as an eluent and how the arium® pro VF system can facilitate this.
This application note from SUEZ outlines the factors that companies should consider when choosing their cleaning validation procedure, highlighting the benefits of TOC analysis over HPLC.
18 April 2019 | By SUEZ
TOC analysis is a widely adopted method for detecting residual product or cleaning agents on manufacturing equipment. Compared to specific methods such as HPLC, TOC can provide better process understanding and efficiency for cleaning validation (CV), verification and continuous monitoring...
A project backed by major pharma will advance the Lab of the Future with proof of concept software to digitise experiment methods…
Instrument agnostic consumables available for an HPLC or LC-MS workflow lab.
Cross checking your HPLC method for impurity profiling with TLC.
Designing a robust cleaning process for pharmaceutical drug manufacturing is critical to successful cleaning validation and verification.
HPLC is a rapid, accurate and sensitive method for determination of pharmaceutical drugs, degradations and impurity profiling. It is a preferred method for analytical characterisation during drug development.
Oligonucleotides must be of high purity when used in molecular biology applications, but efficient purification over a large range of production scales is challenging. The Gilson GX-271 Oligonucleotide Purification System provides a versatile solution for continuous separation, analysis, and desalting of oligonucleotides...
Chromatographic purification of natural compounds presents many challenges to scientists because of the complex nature of the starting matrices that are used in the process...
The advent of High Performance Liquid Chromatography (HPLC) has revolutionised analytical chemistry, greatly enhancing not only the speed of column chromatography, but also the separation and identification capacity of analytes...
8 August 2018 | By SUEZ
The US FDA and European Commission have defined regulations relating to the submission of electronic records in lieu of paper documents, for submission, inspection, and archiving purposes. When ageing analytical equipment is to be replaced 21CFR Part 11 and EU Annex 11 are also topics of discussion. Common questions from…
2 July 2018 | By SCIEX
Different modalities of monoclonal antibodies are pushing the limits of characterization by MS: new critical quality attributes need to be carefully monitored from developability in early phases and then during process development and clinical phases...
Next-Generation UPLC Platform designed to keep pace with evolving laboratory requirements for chromatographic performance...
Visit Booth 2833 to see how Watson-Marlow Fluid Technology Group is able to work with you at every process step...
