News – MedIntegrity – Page 2

May 21

MedIntegrity V10: B2B Applications & Pharma Factory Best Practices

Discover the MedIntegrity V10, an automated multi-method platform ensuring Annex 1 and FDA compliance. It streamlines sterile manufacturing through precise Bubble Point, Diffusive Flow, and Water Intrusion tests while maintaining ALCOA+ data integrity standards.
May 14

Choosing the Right TOC Analyzer for GMP Pharma Labs in 2026

Discover MedIntegrity’s TA Series TOC analyzers, offering UV-oxidation and combustion methods for WFI monitoring and cleaning validation. Ensure 21 CFR Part 11 compliance and data integrity in pharmaceutical water systems.
May 14

Mastering MedIntegrity V10: 2026 Pharma Maintenance Guide

Professional guide for MedIntegrity V10 preventive maintenance. Covers sensor calibration, cleaning protocols, and software validation to ensure Annex 1 and FDA 21 CFR Part 11 compliance in sterile pharmaceutical manufacturing.
May 07

TOC Analysis in Biopharma Water Systems: 2026 Regulatory Compliance Guide

Professional overview of TOC analysis for Purified Water (PW) and Water for Injection (WFI) systems in biopharmaceutical manufacturing. This guide covers USP <643> and EP 2.2.44 regulatory alignment, data integrity requirements for 21 CFR Part 11, and the benefits of online real-time monitoring for cell and gene therapy facilities. Explore technical solutions for continuous organic contamination detection and cleaning validation to ensure operational stability and audit readiness.

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