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Evoqua United States - Canada - EN

CHORUS® Pharma System

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Delivering compliant water for your quality control lab.

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  • Complies with USD Regulation CFR 21 Part 11, USP 643, and USP 645
  • Complies with TOC verification
  • Certified Evoqua service representatives are trained to conduct comprehensive installation and operational qualification of purification systems on-site
  • Digital Record Keeping with secure access
  • Qualification documentation
  • Meets GMP ultra-pure water needs
  • Easily integrated into workflows
Discontinued product
evoqa

Delivering compliant water for your quality control lab.

  • Complies with USD Regulation CFR 21 Part 11, USP 643, and USP 645
  • Complies with TOC verification
  • Certified Evoqua service representatives are trained to conduct comprehensive installation and operational qualification of purification systems on-site
  • Digital Record Keeping with secure access
  • Qualification documentation
  • Meets GMP ultra-pure water needs
  • Easily integrated into workflows
Discontinued product

Description

The CHORUS Pharma System delivers 18.2MΩ ultrapure water from a reliable, intuitive, and simple to use system designed to meet GMP requirements. Easily integrated into existing workflows, this smart pharmaceutical lab water system provides digital record keeping, qualification documentation, and total organic carbon (TOC) and water conductivity measurements required by US pharmacopeia 643 and 645.

The Evoqua Difference

Evoqua improves upon traditional approaches to water management by leveraging decades of experience in water system design. Our unmatched local service network includes 79 service offices in North America, with a travel time of less than 2 hours to 80% of our customers. Our 300+ highly trained service technicians, engineers and customer service representatives are ready to help with all your water needs.

Features

Validations

  • Meets the ultrapure water needs of laboratories operating under the validation conditions stipulated by GMP and Good Documentation Practice.
  • Meets FDA & EU requirements for digital records
  • Supports the TOC sustainability test required by the USP 643
  • Mees the line cell constant required by USP 645
  • Includes all the qualification documentation for typical validation requirements
  • Designed, manufactured, and tested within a Quality Management System and is approved by Lloyds Register Quality Assurance (LRQA), complying with ISO 9001

Compliance

  • CFR 21 Part 11
  • S. Pharmacopeia 643
  • S. Pharmacopeia 645
  • Good Manufacturing Practices (GMP)
  • Total Organic Carbon

Applications

  • Mass Spectrometry
  • Ion & Has Chromatography
  • Ultra-trace and Qualitative Analyses
  • Molecular Biology
  • Cell Cultures
  • Electrochemistry
  • Immunochemistry
  • Laboratory Water Purification

Documentation

Chorus® Pharma System Video

Watch Video