Envair ISO1 -304 Kabinet Keselamatan Pengasing Mudah Alih

Envair ISO1 -304

This listing is introducing 8 No Envair Mobile Isolators of different specifications currently held in our stock

The units are in full working condition and ready for immediate use

Envair Mobile Isolator

Envair Technology is a UK-based manufacturer specializing in clean air and containment solutions for the healthcare, biotechnology, and pharmaceutical industries. Their product range includes a variety of isolators designed to provide controlled environments for handling hazardous substances, ensuring both operator and product safety.

Applications

Envair isolators are widely used in a variety of applications including

Hospital Pharmacies: For preparation of TPN, CIVAS, and aseptic dispensing.

Pharmaceutical Laboratories: Handling of HPAPIs and sterile compounding.

Sterility Testing: Secure, controlled environments for product testing.

R&D Facilities: Safe containment during experimental or early-stage developmen

Key Features of Envair Isolators

Positive and Negative Pressure Models: Envair offers both positive pressure isolators protect the product from contamination and negative pressure isolators to protect the operator from hazardous substances
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Compliance with GMP Standards: Many Envair isolators meet EU GMP Grade A and ISO 5 classifications, ensuring sterile, controlled environments.

Customizable Designs: Envair provides bespoke solutions tailored to specific client needs, including unique dimensions and technical requirements.

Advanced Containment Technology: Isolators are equipped with automated pressure decay leak tests, electromagnetic interlocks for transfer chambers, and integrated decontamination systems.

User-Friendly Controls: Most units include intuitive touchscreen interfaces and PLC-based systems for simple and efficient operation.

Growing Need for Containment with HPAPIs

Demand for personalised medicines containing High Potent Active Pharmaceutical Ingredients (HPAPIs)—particularly in newer super-potent oncology, cardiovascular, and diabetes treatments—is increasing rapidly. These medicines often require shorter turnaround times, forcing pharmaceutical process manufacturers to develop faster, more agile workflows. In such high-risk, high-value settings, a GMP-compliant environment is not optional—it’s critical.

It’s easy to overlook the fact that the people developing, manufacturing, and dispensing these complex drugs are at risk of exposure to harmful, sometimes lethal, compounds. Their safety is paramount, given the essential role they play in maintaining a reliable supply of advanced therapeutics.

Expertise in HPAPI Handling for CMOs & CDMOs

Envair has specialist expertise in helping Contract Manufacturing Organisations (CMOs) and Contract Development and Manufacturing Organisations (CDMOs) safely handle HPAPIs—even within existing non-contained facilities.

Their isolator systems are designed, manufactured, and installed to meet rigorous containment performance levels below 1μg/m³ (OEB 5). Each system is custom-engineered for the specific site and process step—whether it’s weighing, mixing, milling, spray drying, or packaging.

Applications

Hospital Pharmacies: For preparation of TPN, CIVAS, and aseptic dispensing.

Pharmaceutical Laboratories: Handling of HPAPIs and sterile compounding.

Sterility Testing: Secure, controlled environments for product testing.

R&D Facilities: Safe containment during experimental or early-stage development