Cleanroom Products

51. Controlled Expansion Of Supercritical Solutions (CESS®) Technology 4/24/2023

    Nanoform’s award-winning Controlled Expansion of Supercritical Solutions (CESS®) technology is a bottom-up nanoparticle engineering approach that enables the creation of API nanoparticles and can unlock the full therapeutic potential of small molecule drugs.

52. Enhance Resolution For Polymer Analysis Using Non-Aqueous GPC/SEC 6/16/2023

    Phenogel™ Organic GPC/SEC Columns

    Enhance Resolution for Polymer Analysis using Non-Aqueous GPC/SEC

    Phenogel™ size exclusion columns for gel permeation chromatography (GPC) are composed of highly cross-linked styrene-divinylbenzene (SDVB) and achieve high resolution and tight linear calibration curves. Phenogel™ is available in seven different pore sizes, ranging from 50 Å to 106 Å; and a linear bed configuration. Pore size distribution and pore volume are closely controlled parameters in the manufacturing process accounting for the high resolution, tight linear calibration curves, and excellent column-to-column reproducibility. USP L21 packings available.

    • 5 and 10 µm particle sizes
    • Narrow bore (4.6 mm ID) solvent-saver columns available
    • Highly cross-linked for mechanical and chemical stability
    • Temperature stable to 140 °C.
53. API Manufacturing And Material Handling Equipment 5/25/2021

    Active pharmaceutical ingredient (API) manufacturing requires powder handling in a GMP and contained manner. Similar to chemical manufacturing, operations like charging powders into a chemical reactor, emptying a centrifuge or charging and discharging a dryer are standard processes.

54. Pharmaceutical Cleanroom Facilities For Sterile Drug Manufacturing 3/21/2023

    In the spectrum of pharmaceutical manufacturing facilities, injectable product manufacturing facilities represent the most sophisticated and challenging to design, build, qualify and operate, particularly when products manufactured in these facilities are rendered sterile when complete, ready to inject directly into a human. For this reason, very careful consideration must be made when developing such a facility.

55. Cleanrooms And Equipment For CRISPR Drug Manufacturing 6/9/2023

    Revolutionizing Gene Editing: Germfree's Pioneering Cleanroom Solutions Propel CRISPR Manufacturing Forward

    Cleanroom requirements for CRISPR manufacturing necessitate strict adherence to particulate contamination and operational workflows, ensuring safety and product quality in this transformative field. Germfree’s expertise in providing specialized cleanroom solutions supports the effective production of CRISPR-based technologies and their delivery systems. Germfree provides application based fit-for-purpose facilities design to cater to the unique needs of this rapidly evolving sector.

56. Vertical Pharmaceutical Laminar Flow Hoods 11/3/2022

    Germfree’s BVBI Series is engineered to enhance both the performance of the cabinet as well as the overall airflow efficiency of the cleanroom. The air-return is positioned near the bottom of the unit. Germfree’s units are engineered to meet or exceed all advanced specifications for ISO 5 (Formerly Class 100) Laminar Flow Cabinets. These include: ISO 14644-1, US Federal Standard 209E and IES Recommended Practices.

57. bioGO® 53' Mobile Containment Laboratory 11/3/2022

    Germfree’s bioGO® Mobile Biocontainment Laboratories offer the ideal solution for providing surge capacity for laboratory services during periods of emergency. By utilizing a fully equipped/turnkey Mobile Biocontainment Laboratory, facilities are able to rapidly increase their volume without sacrificing capabilities. Each mobile facility is engineered and constructed to meet or exceed relevant CDC NIH BMBL 5th Edition and World Health Organization (WHO) guidelines for BSL2, 2+, or 3 laboratories.

58. Pharmaceutical Cleanroom Design Services 9/2/2020

    Your next cleanroom is more akin to a piece of equipment than a room. Operational efficiencies, compliant flow of materials and personnel, and lifecycle considerations should dictate the selection of your cleanroom partner. AES designers have been engineering functional cleanroom facilities for over three decades, guaranteeing the performance of each and every facility. Our in-house designers work as a team with our cleanroom construction personnel to engineer a cost-effective project while maximizing performance, value, and constructability. The greatest value is realized when AES is integrated into the design team at the start of the project. Early project integration with the AES experts helps the infrastructure team decide what support and cleanroom solutions the clean space requires. Early participation by AES saves design costs, expedites schedule, and eliminates a duplication of services.

59. PTS Powder Transfer System®: Dense Phase Powder Conveying 8/6/2020

    PTS Powder Transfer System® challenges convention by using both vacuum and pressure to move powders as if they were liquids. This eliminates the need for gravity charging and therefore making multi floor processes a requirement of the past.

60. High Shear Batch Mixers For Dispersions And Emulsions 2/7/2023

    High Shear Mixers equipped with the Solids/Liquid Injection Manifold (SLIM) Technology deliver powders in an efficient manner for quick wet-out and complete dispersion into low-viscosity liquids.