Quality Control Solutions

  1. Microbial Culture Media For Quality Control Of Non-Sterile Products 4/7/2022

    Using the correct media is critical to ensure microbiological quality. Explore a portfolio of culture media and substances for sample preparation, microbial enumeration tests, and tests for specified microorganisms.

  2. Residual Seal Force Tester 7/22/2020

    Re-designed from the ground up, the ALL NEW second generation Genesis Residual Seal Force Tester evaluates seal tightness of a sealed parenteral vial by measuring the Residual Seal Force in the stopper/seal combination created as a result of the sealing process.

  3. Performance Validation by Third Party Industrial Hygienists 4/1/2019

    Flow Sciences, a leading provider of containment solutions for laboratory, pilot plant, and manufacturing facilities consults with third party industrial hygienists to conduct in-house Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs) to ensure customers’ products perform at the level they need.

  4. Advanced Product Inspection Technologies For Pharma And Biopharma 11/14/2024

    Pharmaceutical companies face cost, complexity, and speed pressures. Inspection solutions support quality and compliance with fill detection, weighing, foreign body detection, and label verification.

  5. Pharmaceutical Downflow Booth For Freeze Dryers / Lyophilizers 4/3/2019

    Downflow Booth for Freeze Dryer/Lyophilizer designed for product protection when conducting vial-filling and loading vialed product into a freeze-dryer. Features a 304 stainless steel alloy superstructure and perforated stainless steel base.

  6. Biopharmaceutical Isolators And RABS 6/14/2023

    Ensuring Aseptic Conditions and Containment in Pharmaceutical Industry Processes.

  7. Digitalize Your Validation Procedures For Microbial QC Testing 9/28/2023

    Discover a 21 CFR Part 11-compliant digital validation platform designed for conducting IQ & OQ on your microbial QC testing systems dedicated to bioburden testing, sterility testing, and air monitoring.

  8. Quality Standards 3/18/2025

    Learn how our Quality Management System (QMS) can accelerate your project’s path to market and enable the development, manufacture, and delivery of safe and effective products.

  9. Periodic Cleanroom Monitoring 1/30/2020

    TSI’s cleanroom facility environmental monitoring products with built-in redundancy provide the confidence you need to reliably monitor critical processes and demonstrate compliance.

  10. Trusted End-To-End CDMO Partner For Your Journey

    In an increasingly competitive environment, working with the right CDMO is vital for successful drug lifecycle management. We now serve more than half of the world’s leading biopharmaceutical companies, sharing their mission to expedite patient access to life-saving biologics.