Application Notes: Pharmaceuticals
Application Note: Characterizing Nano-pharmaceuticals with FFF-MALS-DLS
Field-flow fractionation coupled to online light scattering detectors determines detailed size and structural information for nanoparticle-based therapeutics.
Separation of Antiretrovirals
Antiretrovirals have come back to the forefront of separation science at this moment in time, as they have found use in the fight against SARS-CoV-2.
Wyatt – Liposome Size, Concentration, and Structural Characterization by FFF-MALS-DLS
Application Note: SEC–MALS Analysis of Exosomes Using the Shodex OHpak SB-806 HQ
LC–MS/MS Solution for Quantitation of Nitrosamine Impurities in Metformin
This application note demonstrates robust and sensitive quantitation of 10 nitrosamines, and the use of the LC–SRM–MS to quantify nitrosamine impurities in metformin.
HRAM LC–MS Method for the Determination of Nitrosamine Impurities
This application note demonstrates fast, highly sensitive quantitation of nine nitrosamines, and the use of the LC–MS method to measure nitrosamine.
GC–MS Analysis of Volatile Green Residual Solvents
The pharma industry is embracing the challenge of sustainability by using greener solvents. A GC–MS method for analyzing 32 green solvents is presented.
Optimizing LC and LC–MS methods with better LC columns
Using fast, efficient HALO® Fused-Core® technology columns and manipulating selectivity quickly develops methods for fast, high-efficiency LC and LC–MS separations.
LC–MS Separation SAMHSA 5 Panel
This application demonstrates HALO® Biphenyl is an ideal choice for high throughput analysis of drug panels, in which isobaric species separation is needed.
Comparative LC Separation of NSAIDs
The separation of non-steroidal anti-inflammatory drugs 60% less time, with better resolution than a typical HPLC column packed with fully porous particles, is demonstrated.
A Commitment to Innovation, Quality, and Experience
This document demonstrates how AMT improves the presentation of the sample to the detector using our Fused-Core® particle design and quality manufacturing.
Evaluation of Recovery of Basic Analytes with Microlute® CP 30 mg Mixed-Mode Strong Cation Exchange (SCX) SPE by HPLC–MS
The 30 mg Microlute® CP Strong Cation Exchange (SCX) 96 well plate compares performance in recoveries and reproducibility against five competitor loose-filled 30 mg SCX products.
Dual Injection (U)HPLC for Analysis of Pharmaceuticals
This application demonstrates the efficiency, throughput, and reliability of a dual-injection system for finished pharmaceutical products and in-process APIs.
Characterization of Recombinant Protein Biotherapeutic Using TSKgel® UP-SW2000 Size Exclusion Chromatography Column In-Line with LenS3TM MALS Detector
Application Note - Shodex HILICpak VC-50 2D for All Essential Amino Acids Detection
App Note: From recent trends in data integrity regulations to Pharma 4.0
This white paper demonstrates a vendor’s perspective on recent trends in regulations and the potential future direction for the industry.
From recent trends in data integrity regulations to Pharma 4.0
Biomimetic HPLC Methods for Drug Discovery
Modified nucleosides, either natural or synthetic, often provide RNA with distinctive properties useful in diagnostics or therapeutics.
An Easier Way to Track Impurities
Learn how impurity-monitoring software can improve your understanding of your process route and help you track fate and purge.
Characterization of Nano-Pharmaceuticals with FFF-MALS-DLS
FFF-MALS-DLS provides the detailed characterization of nano-pharmaceuticals that is essential for development and regulatory filing.
From Data Integrity Regulations to Pharma 4.0
This white paper provides a vendor’s perspective on recent trends in regulations and the potential future direction for the industry referred to as “Pharma 4.0”.
Backup vs. Archive: Why You Need Both
Using Empower CDS and NuGenesis LMS to develop an archive strategy that reduces backup and recovery times and removes manual intervention is demonstrated.
Durable Data for Non-IT
Companies can seek outside help for backup and restore, disaster recovery, and system administration, but responsibility for regulated data remains with the company.
VITAQUEST Streamlines Lab Operations with NuGenesis LMS
VITAQUEST, a contract manufacturer of dietary supplements, used NuGenesis LMS to automate its workflows, improve lab efficiency, and reduce the risk for data errors.
Empower Cloud Streamlines Pharmaceutical Operations
This study shows how coupling Waters’ Empower CDS with cloud technology allowed a pharmaceutical company to streamline its global operations and connect each of its labs.
Role of Empower CDS in Electronic Record Regulation Compliance
This white paper explains the 21 CFR Part 11 and EU EudraLex Annex 11 compliance readiness of Waters Empower Software for the regulated scientific laboratory.
Managing Empower Data with NuGenesis LMS
This case study demonstrates the advantages of pairing Empower CDS with NuGenesis LMS to improve the availability of your CDS data and maximize its effectiveness.
CRO Increases Advantage by Implementing Empower CDS
A&M Stabtest, an independent CRO in the pharmaceutical industry, reduced time-consuming and error-prone manual steps in the chromatographic testing process.
CDMO Advances Data Integrity and Lab Productivity
An investment in Waters NuGenesis LMS helped a global pharmaceutical CDMO meet demands for data integrity regulatory compliance and laboratory management needs.
Method Lifecycle Management Drives Development at CDMO
This study demonstrates Waters ACQUITY UPLC with PDA/QDa technology and Empower Software were integral to successful method lifecycle management at Hovione, a global CDMO.