Application Notes: Pharmaceuticals

From recent trends in data integrity regulations to Pharma 4.0

November 24, 2020

This white paper demonstrates a vendor’s perspective on recent trends in regulations and the potential future direction for the industry.

Biomimetic HPLC Methods for Drug Discovery

November 18, 2020

Modified nucleosides, either natural or synthetic, often provide RNA with distinctive properties useful in diagnostics or therapeutics.

An Easier Way to Track Impurities

November 04, 2020

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

October 16, 2020

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

October 14, 2020

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

October 12, 2020

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

October 12, 2020

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

October 12, 2020

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

October 12, 2020

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

October 12, 2020

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.