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PURELAB® Pharma Compliance

ELGA LabWaterAvailable: Worldwide

Bringing ELGA's ultrapure water purification to GXP Quality Control Laboratories

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Description

The Pharma Compliance delivers a lab water solution focused on building the perfect relationship between discovery, production and traceability, resulting in an intuitive, efficient and compliant purification system.

PURELAB Pharma Compliance is packed with innovative features optimised for QC laboratories. It offers all the necessary purification, software capabilities, qualification documentation and online support services necessary for the validation required to meet Good Manufacturing Practice (GMP). It includes secure software providing the evidence to meet FDA and EU standards for digital record keeping. Purification processes fulfil United States Pharmacopeia standards 643 and 645. Qualification documents provided enable the unit to support labs subject to validation under GxP.

Application NoteGeneral Lab

Water needs in pharma quality control

Water is one of the most widely used substances in the pharmaceutical industry. It functions as an ingredient, a cleaning agent, a reagent, a solvent, and a product, throughout the drug discovery process, from the initial identification of potential drug targets, all the way to the manufacture and quality control of the final product. In this application note, ELGA LabWater outlines common challenges and outlines the solutions to using water across a multitude of laboratories.

Pharma compliance

Watch this presentation by David Grant, Global Product Manager at ELGA LabWater, titled: Pharma compliance. This talk was presented at the SelectScience® Virtual Biopharmaceuticals Summit 2022.


Video

The NEW PURELAB® Pharma Compliance 2022

ELGA is now introducing the PURELAB® Pharma Compliance - bringing ELGA’s water purification to GxP Quality Control laboratories.

PURELAB® Pharma Compliance is packed with innovative features optimised for QC laboratories. It offers all the necessary purification, software capabilities, qualification documentation and online support services necessary for the validation required to meet Good Manufacturing Practice (GMP).

Pharma Compliance includes secure software providing the evidence to meet FDA and EU standards for digital record keeping. Purification processes fulfill United States Pharmacopia standards 643 and 645. Qualification documents provided enable the unit to support labs subject to validation under GxP.

The ultrapure water system meets your laboratories needs, with minimal intervention, improved efficiencies, and a contemporary style to compliment any modern laboratory.

The highly competitive total cost of ownership, robust traceability, and great ergonomics combine to create a simply compliant, simply effective, and simply transparent solution.


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