Quality Control Solutions

  1. Custom Bulk Packaging For Pharmaceutical Raw Materials 3/8/2023

    Learn about a custom chemical bulk packaging service that offers high-purity raw materials in precise amounts in a variety of ready-to-use configurations for cGMP manufacturers.

  2. Master Control Quality Excellence 6/30/2026

    An interconnected digital platform unifies quality documents, training, and corrective actions. Learn to eliminate manual gaps and use automated metrics to drive long-term operational excellence.

  3. Container Closure Integrity Of Parenteral Products 7/9/2020

    The United States Pharmacopeia USP 1207 guidance has been revised, encouraging the preference to deterministic, quantitative, and reliable non-destructive technologies to comply with quality standards.

  4. Cleanroom Capabilities And Expertise

    Learn how the right partner can ensure that your facilities maintain cGMP-compliance and help establish the correct testing program and parameters based on your needs.

  5. Automate Your Microbial QC Workflow 8/25/2026

    See how automated microbial quality control reduces manual handling, accelerates growth detection, and preserves colonies for identification while supporting faster manufacturing decisions.

  6. Cell Therapy From Culture To Cure: Enabling Your Path From Discovery To Commercialization 6/10/2025

    Realize the full potential of your cell therapy research. Experience end-to-end support to overcome developmental complexities, helping you to efficiently and safely commercialize your groundbreaking treatments.

  7. Flexible And Precise Accumulation Solutions 8/7/2024

    Optimize your line efficiency with accumulation between the upstream and downstream machines. Our accumulators let you decouple two machines, meaning you can run different equipment at varying speeds while still maintaining balance in the event of upstream or downstream stoppages.

  8. Software For Trusted And Efficient Data Recording

    Discover your digital QC companion for sterility testing and other regulated processes. Ensure full traceability and regulatory compliance with contemporaneous, automatic, and complete recording of QC testing data.

  9. General Processing Platform Isolator 2/27/2026

    Optimize your aseptic workflows with this adaptable containment platform, featuring flexible airflow and pressure controls to ensure rigorous sterility for diverse pharmaceutical processes.

  10. BioPass™ Pass Through: Seamless Transfers With Built-In Sterilization To Prevent Cross-Contamination 2/27/2026

    Streamline large equipment transfers with integrated bio-decontamination. This airtight system ensures a log 6 microbial reduction while maintaining strict ISO Class 5 cleanroom integrity.