Agilent MicroLab Software with Spectroscopy Configuration Manager and Spectroscopy Database Administrator (SCM/SDA)
This technical note describes features and functionality of Agilent MicroLab software (version 5.2 and later) in combination with SCM and SDA for data management and electronic traceability, which enable customers to implement the guidelines of 21 CFR Part 11.

Agilent Cary 630 Laboratory FT-IR and Agilent 4500 Portable FT-IR Systems for Detection of Counterfeit Pharmaceuticals
This application note demonstrates the effectiveness of Agilent compact and portable FT-IR systems for detecting counterfeit pharmaceuticals with three examples: ethambutol hydrochloride, cephuroxime axetil, and atorvastatin calcium.

Agilent Cary 630 FT-IR Spectrometer Quickly Identifies and Qualifies Pharmaceuticals
This application note describes a very sensitive classification method, partial least squares–discriminant analysis (PLS-DA), incorporated in Agilent innovative MicroLab software, to classify and qualify materials of interest with greater sensitivity and specificity than possible with simple library search methods.

Agilent Cary 630 FT-IR Pharmacopoeia Compliance
This application note demonstrates how Agilent's Cary 630 FT-IR easily meets the specifications of the US, European, Japanese, Chinese, Indian, and International Pharmacopoeia. Its combination of compact size, design, intuitive and regulation-compliant software makes the Cary 630 FT-IR an ideal instrument for pharmaceutical quality control.

Good Laboratory Practice: Agilent Cary 8454 UV-visible Spectroscopy System
This note looks at specific components that require validation; the instrument, software, and validated test methods, and describes the features of the Agilent Cary 8454 UV-visible system that is designed to meet the requirements of both initial and recurrent validation.

The Diode Array Advantage for Pharmaceutical QA–QC
The Agilent Cary 8454 UV-visible system is ideal for regulatory pharma QA and QC applications, and can acquire a complete spectrum in less than 1 s. This technical note outlines both applications-based and technical considerations for choosing a diode array UV-vis

QA–QC Pharmaceutical Solutions— Cary 8454 UV-visible Spectroscopy System
This note describes how the design of the Cary 8454 UV-vis exceeds performance requirements stipulated by global pharmacopeia guidelines including USP and EP/BP. Configured for compliance, with 21 CFR Part 11, the instrument performs multi-wavelength analysis, time-based kinetics assays, and routine QA and QC measurements.

Enhancing Confidence in Compliance
This note highlights OpenLAB ECM Compliance Pack for UV-vis benefits such as efficient data storage and retrieval, security, data integrity and traceability, and 21 CFR Part II compliance.