WFI stands for Water for Injection. It is a highly purified water used in the preparation of medicines where water is the vehicle, or for washing equipment that comes into contact with parenteral products.

Why is a dedicated storage and distribution system necessary for WFI?

A dedicated system ensures the WFI maintains its high purity after generation, preventing re-contamination during storage and delivery to points of use, which is critical for patient safety.

What are the key components of a WFI storage and distribution system?

Key components typically include a storage tank, a circulation pump, heat exchangers for temperature control, a piping loop, and various instrumentation for monitoring water quality.

How is microbial control maintained in these systems?

Microbial control is commonly achieved through continuous circulation at elevated temperatures (hot loop), or through periodic hot water or steam sanitisation for ambient loops.

What regulatory standards apply to WFI systems?

WFI systems must comply with pharmacopoeial standards (e.g., EP, USP, JP) and Good Manufacturing Practice (GMP) guidelines, including those from regulatory bodies like the MHRA and FDA.

Used BWT LOOPO WFI Storage and Distribution System - WFI Generation & Storage Systems, photo 1

Used BWT LOOPO WFI Storage and Distribution System - WFI Generation & Storage Systems, photo 2

Used BWT LOOPO WFI Storage and Distribution System - WFI Generation & Storage Systems, photo 3

Used BWT LOOPO WFI Storage and Distribution System - WFI Generation & Storage Systems, photo 4

Used BWT LOOPO WFI Storage and Distribution System - WFI Generation & Storage Systems, photo 5

Used BWT LOOPO WFI Storage and Distribution System - WFI Generation & Storage Systems, photo 6

Used BWT LOOPO WFI Storage and Distribution System - WFI Generation & Storage Systems

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BWT LOOPO WFI Storage and Distribution System

Name: BWT LOOPO WFI Storage and Distribution System
Brand: BWT
SKU: 6073751
Availability: InStock

Prix : Prix sur demande auprès du vendeur

BWT LOOPO WFI system ensures reliable storage and distribution of high-purity water for injection, supporting pharaceutical and bioprocessing operations

Cambridgeshire, United Kingdom

À 5 773 km

Numéro de modèle

LOOP0

Numéro de stock

6073751

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Informations types pour cette catégorie de machines. Vérifiez toujours les détails auprès du vendeur.

Pharmaceutical manufacturing for drug formulation and active pharmaceutical ingredient (API) production.
Biotechnology and life sciences for cell culture media preparation and buffer solutions.
Healthcare facilities for sterile processing and laboratory use.
Cosmetics industry for high-purity ingredient formulation.

Typical capacity: Storage tanks for WFI systems commonly range from several hundred to several thousand litres, depending on process demand.
Power supply: Units of this type typically require a three-phase industrial power supply, commonly 400V, 50Hz, with specific amperage requirements varying by pump and heating element size.
Operating temperature: WFI storage and distribution systems often operate at elevated temperatures (e.g., 80-90°C) for microbial control, or ambient with periodic sanitisation.
Materials of construction: Product-contact surfaces are typically constructed from 316L stainless steel, with an electropolished finish to meet pharmaceutical standards.
Control system: Modern systems commonly feature PLC-based control with HMI for monitoring parameters such as temperature, pressure, flow, and conductivity.
Sanitisation method: Systems are typically designed for hot water sanitisation (HWS) or steam-in-place (SIP) to maintain WFI quality.

WFI stands for Water for Injection. It is a highly purified water used in the preparation of medicines where water is the vehicle, or for washing equipment that comes into contact with parenteral products.

WFI generation and storage systems are considered essential infrastructure in pharmaceutical manufacturing. Buyers typically prioritise systems with verified maintenance records, as reliability and consistent water quality are critical. Key considerations include capacity requirements, sanitisation capability, and compliance with relevant pharmaceutical standards. Industry sentiment favours units demonstrating robust construction and proven track records in similar production environments. Used systems often provide good value when sourcing from established manufacturers with documented performance history and complete documentation of previous operating conditions and service schedules.

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