Critical Environments Solutions

  1. Cell & Gene Therapies: Automating the Future of Regenerative Medicine 9/1/2026

    Scaling cell and gene therapies requires transitioning manual workflows to automated, closed environments. Modular platforms optimize cleanroom footprint, accelerate production, and ensure consistent batch quality through real-time monitoring and seamless digital traceability.

  2. Leading Solutions For Air And Gas Monitoring

    Viable air monitoring is a crucial component of contamination control strategies in pharmaceutical manufacturing. Find out what advantages the MAS-100® microbial air and compressed gas samplers offer.

  3. Pharmaceutical Cleanroom Environmental Contamination Monitoring 11/23/2021

    Monitor your viable and non-viable particles according to the most recent regulatory requirements. Count, report, document and manage your pharmaceutical environmental monitoring data meeting 21 CFR Part 11 data integrity requirements.

  4. Isolators For Aseptic Manufacturing 5/6/2016

    Extract Technology aseptic isolators are designed to allow operators to perform aseptic processes in a sterile environment providing assurance of process integrity.

  5. Pre-Designed Pharmaceutical Cleanroom: Express 15K, 8 Months Delivery 9/9/2020

    Faciflex Express is a pre-designed cleanroom solution that delivers a commissioned cleanroom in as little as 6 months. Pre-designed standard cleanroom layouts are the next generation for snap together installation of modular panel systems. Faciliflex Express has 3 models 5k, 15k, and 30k representing cleanrooms of approximately 5,000, 15,000, and 30,000 square foot.

  6. Kinetex® Core-Shell Technology Columns For HPLC or UHPLC Methods 6/9/2023

    The power of ULTRA-Performance on any LC System

    • Higher throughput without sacrificing resolution
    • Reduce solvent usage with faster analysis
    • Lower levels of detection and quantitation
  7. Stability Testing – Onsite Preclinical Services To Support Your Product Development 7/29/2024

    Natoli Scientific’s preclinical stability studies represent a critical facet of our pharmaceutical testing services, providing essential data on the shelf life and storage conditions of drug candidates. These studies are expertly designed to evaluate physical, chemical, and microbiological stability, ensuring that formulations retain their safety, efficacy, and quality over time. Our state-of-the-art facilities simulate various environmental conditions to scrutinize the integrity of products under stress-testing scenarios. The results gleaned from our stability studies guide the development of robust drug formulations and packaging, aid in regulatory submissions, and lay the groundwork for successful commercialization.

  8. Pharmaceutical Facility Monitoring System 12/1/2022

    Facility Monitoring System with industrial control systems assures data integrity, process automation, simplicity of use, and data integration.

  9. Evoqua Water Technologies RO/DI Water System 4/30/2026

    Used Evoqua Water Technologies RO/DI Water System, with (6) tube RO system, prefilter, 60 hp Grundfos pump, skid mounted with RIO Panel and power distribution panel, CDI continuous electrodeionization unit, (6) IonPure LX units, Carbon Tower bed, main control panel with HMI, serial# 10262039, built 2023.

  10. QA Microbiology Isolators: ST-IS Series 7/6/2026

    Designed for pharmaceutical quality control and microbiology laboratories.