Cleanroom Products
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Annex 1-Compliant Real-Time Viable Particle Counter
12/15/2022
What Is Annex 1 and Why Is It Important? Annex 1 is a GMP document published by the European Commission and dedicated to the manufacturing of sterile products. All pharmaceutical companies that produce sterile products must comply with these regulations. The document is a joint initiative between the EMA and PIC/S.
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Sand Media Filters
5/12/2023
These sand media filters bring a high-performance solution to the toughest dirty water conditions.
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USP <797> And USP <800> Mobile Compounding Pharmacies
1/25/2023
Germfree’s Compounding Pharmacy equipment and bioGO® Mobile, Modular Pharmacies are Offsite-built, Compounding-ready and available in standard and custom configurations, for sale or lease.
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Gravimetric Powder Filler: Fill2Weight
3/26/2025
Fills syringes, vials, cartridges, capsules and custom containers at speed with aseptic powder micro-dosing technology.
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Syringes
8/22/2021
Stevanato Group through its historical brand Ompi provides a wide range of washed, siliconized and pre-sterilized EZ-fill® syringes systems. Available in a range of sizes from 0,5 ml to 5 mL with staked needle, Luer cone or Luer lock adapter. Bulk syringe systems are available with or without staked needle and provided in trays.
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Cleanrooms And Equipment For Cell Therapy Drug Manufacturing
6/9/2023
Delivering on the promise of cell and gene therapy through Germfree products and services.
Germfree Laboratories offer advanced modular and mobile facilities, equipment, and comprehensive services for cell therapy manufacturing. Acknowledging the complexity of personalized treatments, Germfree’s adaptable solutions optimize production processes, ensuring aseptic conditions, scalability, and compliance with regulatory standards. This enables efficient, high-quality cell therapy delivery to patients in need, supporting manufacturers in overcoming industry challenges.
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Automated, Single-Use System For Clinical And Commercial LNP Production
7/21/2023
The NanoAssemblr® commercial formulation system is an automated, single-use system for the clinical and commercial production of lipid nanoparticles (LNPs) under cGMP conditions. Designed for efficient changeover and robust manufacturing processes, the system enables operational flexibility and standardized manufacturing of genomic medicines.
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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.
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Wet Nanomilling And Vial Filling
9/9/2024
Nanomilling revolutionizes drug delivery by reducing particle size to enhance solubility, bioavailability, and therapeutic efficacy, addressing the challenges of poorly water-soluble APIs.
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Biopharmaceutical Isolators And RABS
6/14/2023
Ensuring Aseptic Conditions and Containment in Pharmaceutical Industry Processes.