- Vekamaf.com Poland https://vekamaf.pl/technologies/systemy-kontroli-wilgotnosci/ Inżynierowie Linii Produkcyjnej Mon, 22 Dec 2025 09:10:01 +0000 en-US hourly 1 https://wordpress.org/?v=6.9 Linia napełniania fiolek i system liofilizacji https://vekamaf.pl/urządzenia/linia-napelniania-fiolek-i-system-liofilizacji/ https://vekamaf.pl/urządzenia/linia-napelniania-fiolek-i-system-liofilizacji/#respond Tue, 03 Sep 2024 16:02:39 +0000 https://vekamaf.com/equipment/vial-filling-line-and-freeze-dryer-system For seamless drug production, integrate reliable vial filling with precision freeze drying, designed to handle high-potency biologics and live vaccines under strict bio-decontamination and environmental controls. Fills, Freeze Dries, and Isolates Vials The Vial Filling Line from Telstar integrates a freeze dryer with an aseptic isolator, addressing the stringent sterility needs for biopharmaceutical and vaccine […]

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]]> For seamless drug production, integrate reliable vial filling with precision freeze drying, designed to handle high-potency biologics and live vaccines under strict bio-decontamination and environmental controls.

Fills, Freeze Dries, and Isolates Vials

The Vial Filling Line from Telstar integrates a freeze dryer with an aseptic isolator, addressing the stringent sterility needs for biopharmaceutical and vaccine manufacturing. Designed for high potency drug production, this system automates vial filling, freeze drying, and bio-decontamination processes under Grade A unidirectional airflow. It features an automatic loading and unloading system, reducing manual handling and contamination risk. With integrated temperature and humidity control, and RFID glove testing, it ensures precise environmental conditions for handling sensitive products like trastuzumab and live attenuated vaccines. Compliant with GMP standards, the line supports remote monitoring and offers reliable isolation with return BIBO HEPA filters. Installation supports seamless integration into existing production lines, providing operational efficiency and scalability.

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]]> https://vekamaf.pl/urządzenia/linia-napelniania-fiolek-i-system-liofilizacji/feed/ 0 Aseptyczny system izolatora do napełniania strzykawek https://vekamaf.pl/urządzenia/aseptyczny-system-izolatora-do-napelniania-strzykawek/ https://vekamaf.pl/urządzenia/aseptyczny-system-izolatora-do-napelniania-strzykawek/#respond Tue, 03 Sep 2024 16:02:21 +0000 https://vekamaf.com/equipment/aseptic-syringe-filling-isolator-system Ensure product sterility and precision with a cutting-edge solution for aseptic syringe filling, designed to optimize airflow and contamination control, while maintaining stringent environmental parameters for your sensitive processes. Ensures Sterile Syringe Filling and Decontamination The Aseptic Syringe Filling Isolator System from Telstar is engineered to enhance sterility in biopharmaceutical and pharmaceutical production, specifically designed […]

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]]> Ensure product sterility and precision with a cutting-edge solution for aseptic syringe filling, designed to optimize airflow and contamination control, while maintaining stringent environmental parameters for your sensitive processes.

Ensures Sterile Syringe Filling and Decontamination

The Aseptic Syringe Filling Isolator System from Telstar is engineered to enhance sterility in biopharmaceutical and pharmaceutical production, specifically designed for aseptic syringe filling. This system features a multi-chamber design that enables seamless integration into pilot-scale production lines, ensuring sterile conditions with ISO Class 4.8 (grade A) air cleanliness. Equipped with a recirculatory unidirectional airflow system and an independent decontamination chamber, it provides robust contamination control. Ideal for producing sterile injectables, pre-filled syringes, ophthalmic solutions, and pilot-scale sterile batches, it utilizes Integral Telstar ionHP+ bio-decontamination for high purification levels. With automated air temperature and humidity control, it maintains <3% RH, enhancing process consistency. RFID glove testing and viable/non-viable monitoring ensure compliance with stringent GMP standards. The system supports easy integration with existing equipment through its configurable design, facilitating efficient transitions and minimal downtime.

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