ザルトリウス・ステディム・ジャパン Official site

Filtration, storage, and transportation in all process stages. Take Your Facility Into The Future.

By downloading the PDF, you can view the following information regarding Flexsafe 2D and 3D: 2D media preparation 3D media filtration, storage, and transportation 2D buffer preparation 3D buffer filtration, storage, and transportation 2D cell harvest and downstream intermediates 3D cell harvest and downstream intermediates filtration, storage, and transportation 2D active pharmaceutical ingredient 3D active pharmaceutical ingredient filtration, storage, and transportation 2D formulation adjustment 3D formulation filtration, storage, and filling

Please check the Japanese version catalog for a significant increase in operability and stirring power!

<Features> ▪ Providing unprecedented performance and quality assurance ▪ Control over the entire manufacturing process ▪ Quality assurance for fluid contact components ▪ Validation and quality assurance ▪ Guaranteeing the integrity of container closures ▪ Safe and reliable handling and shipping solutions from 5L to 500L ▪ Safe, self-expanding robust solutions

A fast, accurate, reliable, and safe system.

The Takeone sterile sampling device is a pre-assembled single-use sampling solution. The Takeone sterile sampling devices in 25 mm, 1.5", and 2" sizes have completely closed sampling lines with 3, 5, or 9 tubes. Takeone ensures the precise collection of the required samples, leading to accurate analytical results.

A particulate reduction program that comprehensively addresses particulate matter risks with the aim of advancing discussions based on objective data rather than subjective risks.

▪ VDI (Visual Inspection) Inspection of visible defects, including visible particles, in all bag chambers. ▪ VPT (Particle Extraction and Measurement) Monitoring of visible particles on representative products using liquid extraction and microscopic counting. ▪ Lot-based VPT (Optional Service) Monitoring of visible particles extracted from actual manufacturing lots using liquid extraction and microscopic counting. VPT is just one step in Sartorius' particle reduction program. By monitoring events and trends over time, we can deepen our understanding of the sources and nature of particulate matter. Sartorius can embark on continuous improvement to reduce visible particle levels over time by combining other steps of the particle reduction program. VPT is one of the pillars to ensure consistency in quality between batches, leading to a reduction in risks related to patient safety. This new approach continues to support the use of SUS in critical applications.

Solutions to ensure the safety of regulations.

Zaltrius has been providing validation services to the biopharmaceutical industry for over 25 years. We have a deep understanding of the regulatory landscape and adopt a tailored approach for all our clients.

Pioneer of filtration sterilization

In this catalog, you can find information on the main applications, advantages, sizes, materials, characteristics, and product numbers for the following products: ▪ Sartopore 2 Series ▪ Sartopore Platinum ▪ Sartobran P ▪ Sartolon Additionally, we provide detailed information about our "Filtration Performance Testing Service," which includes selecting the most suitable filter for your chemical solutions and conducting scale-down tests for size determination at no charge.

Achieve both efficiency improvement and cost reduction. A free testing service that identifies the optimal type and size of filter for the chemicals used.

■ Testing Method: Constant Pressure Filtration Test ■ Order: Please contact us directly or reach out to our sales team ■ Testing Date: To be determined after approval of the test plan, according to the customer's convenience ■ Preparation for Testing: No preparation needed for our filters (preparation is required for filters other than ours) ■ Implementation of Testing: If conducted at the customer's site, the work is generally completed during working hours (in some cases, it may require a stay of several days) ■ Test Report: Submitted approximately 7 days after the test (results can also be presented in a preliminary format)