Video: Automation for E&L analysis
Get a quick view of sample preparation and automation gear for E&L analysis.
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Get a quick view of sample preparation and automation gear for E&L analysis.
This presentation will provide method development guidance for the extraction and quantification of analytes using headspace SPME.
Combining the world's fastest proteomics instrument with over 25 years of MALDI experience.
The timsTOF Pro with diaPASEF enables deeper proteome coverage in a single 4D shotgun proteomics experiment, with highly reproducible qualitative and quantitative results - making it a near-ideal mass analyzer for proteomics.
This seminar describes different membrane characteristics and provides guidance in selecting the right filtration devices for sample preparation following in vitro dissolution.
In this webinar, we will introduce you to the microbial environmental monitoring in production isolators. You will learn how to be compliant and ease your workflow.
When it comes to microbial contamination testing, false results can waste valuable time.
Testing for pyrogens is a critical step in ensuring the safety of parenteral pharmaceutical products and medical devices.
Microbial risk in pharmaceutical process is not limited to living microorganisms and intact microbial cells.
Many Pharmacopeia materials contain water as hydrates or in adsorbed form.
The ICR Swab is a unique system for environmental monitoring of dry surfaces, such as filling needles, equipment recesses, uneven surfaces and tubing in clean rooms and isolators.
Introduced at ASMS 2019, the new SYNAPT XS provides ultimate flexibility offering greater freedom of analytical choice to support scientific creativity and technical success for any application.
Our culture media are the reliable and convenient choice for aseptic process simulation and include Ready-to-use and Dehydrated Culture Media to meet the specific needs in the pharmaceutical industry.
The European Regulatory Framework for Medical Device field is changing with the release of the new Regulation. The MDR will replace the existing Directives and it will be fully in force in May 2020.
Overview on how ionBench products can help LC/MS users with dedicated furniture for their instrumentation