Changes to GMP force cleanroom re-classifications
Cleanroom users claiming compliance to cGMP and/or GMP will have to consider a new rule, ISO 14644-1:2015, when next re-qualifying…
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Reclaim Your Wasted Time with the new Agilent 5800 ICP-OES
Agilent ICP-OES Instruments for atomic spectroscopy deliver uncompromised performance, speed and ease of use in ICP-OES and…
Your Genuinely Better Solution for Volatiles Analysis
A Reliable and Robust Workhorse that Maximizes Throughput and Minimizes Error to Deliver the Performance, Simplicity, and…
Elemental Impurity Analysis in Pharmaceuticals: Validating performance of an Agilent 7800 ICP MS
Worldwide, regulatory authorities are responsible for ensuring that pharmaceutical products are both effective and safe. To…
How to Comply with the 2017 Version of USP <1058>
Agilent offers a comprehensive set of compliance services, including instrument and software qualifications (IQOQ, OQ, and RQ)…
Minimize Disruption, Maximize Uptime
Agilent CrossLab relocation services do more than just move lab equipment. We can deliver a complete lab relocation, a single…
Many instrument models, one service provider
Agilent’s CrossLab services provide laboratories with comprehensive maintenance coverage to suit their specific needs and budget.…
Streamlined Core Facility Management
Agilent CrossLab iLab core facility management is a web-based enterprise software solution composed of a base software suite and…
Ensure Compliance and Data Integrity with Agilent Computer System Validation Services
Agilent CrossLab computer system validation (CSV) is the foundation for data integrity compliance, which is the main focus of…
Pharmaceutical Analysis Using UV-Vis: Compliance with USP Chapter <857>, and Ph. Eur. 2.2.25
Meeting the requirements of the global pharmacopeias with the Agilent Cary 3500 UV-Vis: The United States pharmacopeia (USP) and…
Validation of On-line Total Organic Carbon Analysers for Release Testing Using ICH Q2
As the pharmaceutical industry seeks to reduce the number and associated costs of quality control laboratory tests, reliance on…
IMPLEMENTING A UNIFIED LAB MANAGEMENT SOLUTION
THE CUSTOMER: A GLOBAL LEADER IN
BIOTECHNOLOGY THAT IS ADVANCING SCIENCE
AND INNOVATION
Agilent Cary UV Workstation Software for Cary 3500
US FDA Part 11 in Title 21 of the Code of Federal Regulations (CFR), and its EU analog, Eudralex Chapter 4, Annex 11, describe the…
Agilent Cary 3500 UV-Vis: Multiply your experimental possibilities
The Agilent Cary 3500 UV-Vis spectrophotometer offers photometric performance together with unique measurement capabilities while…
Verifying Raw Materials Using Spatially Offset Raman Spectroscopy- The New Agilent Vaya Raman
Spatially offset Raman spectroscopy (SORS) is a powerful technology used for identifying materials inside unopened packaging. SORS…
Reducing the cost of quality with the Agilent Vaya Raman system
With profit margins in the pharmaceutical industry under ever increasing pressure, manufacturing groups are incentivized to…
Root cause investigation for pharmaceutical water systems
In their 21CFR guidance, the FDA emphasise the importance of corrective and preventative action (CAPA) for any deviations…
Beckman Coulter’s New Line of Centrifuges Provides Support for 21 CFR Part 11 Compliant Laboratories
As technology and software advance, security and protection of data is becoming increasingly important to ensure a properly…
Avanti JXN Series – Complete solution for protein purification workflow.
Purified proteins are required for many proteomics applications such as X-ray crystallography, NMR, mass
spec, and in vitro…
A Beginner’s Guide to Bioprocess Modes – Batch, Fed-Batch, and Continuous Fermentation
In this application note, we explain the differences between batch, fed-batch, and continuous fermentation and how these influence…