Ultrapure lab water designed for pharmaceutical compliance and QC efficiency
Features for Pharmaceutical Compliance
Secure software offers a range of admin, security and data features providing evidence to meet FDA (FDA 21 CFR Part 11) and EU (EUDRALEX Annex 11) standards for digital record keeping.
Purification processes fulfil United States Pharmacopeia standards 643 and 645.
Supported by a global network of service teams with significant experience of supporting laboratory equipment subject to validation under GMP.
Space saving to enhance QC output, designed to be modular and stackable to save space.
Cost effective design delivering water to support QC tests necessary to validate drug purity in pharma manufacturing. Consumables are designed to minimise cost and environmental waste. ELGA delivers lower total cost of ownership that can be easily integrated into any laboratory.
The PURELAB® Pharma Compliance system delivers a complete pharmaceutical lab water solution - combining advanced purification, intuitive software, and secure data handling to meet the strict demands of GxP, FDA 21 CFR Part 11, and EU Annex 11 regulations. This system is ideal for QC laboratories, pharmaceutical manufacturing, and any environment requiring ultrapure water for pharmaceutical laboratories.
Bringing ELGA's ultrapure water purification to GXP Quality Control Laboratories
PURELAB® Pharma Compliance is a purpose-built lab water purification system designed to meet the rigorous demands of GxP-regulated pharmaceutical environments. Whether you're validating drug purity or conducting routine QC analysis, this system delivers: