Reduce Regulatory Risk with Industry Best Practice
All analytical testing is performed to satisfy regulatory requirements or business needs. However, regulatory requirements are not…
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Transform your End-Product Testing- Quantification of Tablets Containing Multiple APIs Using…
The ability to predict multiple constituents of a final dosage form in one fast, nondestructive measurement can reduce analysis…
Wondering which LC Column should I choose?
The InfinityLab Poroshell 120 family has grown to 18 chemistries—including new phases for chiral and HILIC separations. Now, you…
Improving Operations Management of Core Laboratories
iLab is a cloud-based laboratory management solution that allows scheduling of time on equipment, allocation of staff to projects,…
Best practices for LC (Liquid Chromatography) – Immediately Increase Efficiency in Your Lab
Want new insights into reliable, efficient LC operations?
Then you need to download our exclusive e-book: Best Practices for…
A single-source solution to your service needs: Agilent CrossLab Multi-Vendor Instrument Services
When you need comprehensive repair, preventive maintenance, qualification, or relocation support for your LC, GC, atomic and…
Specifying Non-Viable Particle Monitoring for Aseptic Processing
Major pharmaceutical companies are investing in new biologics, most of which will be manufactured using aseptic processing.…
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…
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…
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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…