Containment patient isolators. Medical search. Frequent questions

Applications include transfer from an external area to a cleanroom, transfer from within a cleanroom to isolators used as barriers or transfer inside incubators. (bioworld.com)
It often houses a "non-cleanroom grade", HD storage refrigerator and all the HD inventory storage, because it is the only containment room. (asepticenclosures.com)
Introducing an automated filling with closed restricted access barrier system (cRABs) within an existing cleanroom facility allows one to focus on developing modular single-use systems, including isolator containment, to maximize product diversity and expedite process turnaround. (curiaglobal.com)
Over the years, Central Research Laboratories (CRL), for example, has created a full stable of RTP technologies that have been designed around the capabilities of an innovative double-door transfer system, which allows all types of materials to be rapidly transferred into and out of cleanroom, isolation chamber, or glovebox without breaking containment. (medicaldesignbriefs.com)
Our SimpleSeal™ luminaires are designed to maintain the particulate and contaminate requirements of cleanroom and containment areas, while being easy to install and inexpensive to maintain. (cleanroomcompanydirectory.com)

The purpose of this document is to establish an industry-based minimum set of testing criteria appropriate for all Compounding Isolators used pursuant to USP Chapter 797 1. (escolifesciences.us)
Compounding Isolators consist of Compounding Aseptic Isolators used for compounding sterile preparations and Compounding Aseptic Containment Isolators used for compounding sterile hazardous drug preparations in pharmacy applications. (escolifesciences.us)

Bioquell offers unmatched decontamination solutions, from bioburden removal in compounding aseptic containment isolators (CACIs) to entire rooms within your pharmacy. (tecture.net)
Bioquell offers unmatched solutions from compounding aseptic containment isolators (CACIs) to decontaminating your entire room to maintain acceptable particle counts. (amazonaws.com)

Do you need a reliable and compliant solution for active viable air monitoring in your isolator or RABS? (rapidmicrobiology.com)
Barrier systems such as isolators or RABS play a fundamental role in the protection of people and products in pharmaceutical production. (manufacturingchemist.com)
The use of isolators, restricted access barrier systems (RABS) and the use of SBVs has increased in recent years due to their ability to separate drug products from operators and limit manual intervention. (cleanroomtechnology.com)

How do you successfully implement high containment in pharma manufacturing? (pharmaceuticalmanufacturer.media)
This double chamber negative pressure designed isolator installed in ATEX zone 1 area provides a high containment environment during the automated filter dryer discharge of highly potent APIs of a Minimum Ignition Energy (MIE) less than 10 mJ. (pharmaceuticalmanufacturer.media)
High containment level is maintained by using an airlock for material in- and outlet. (pharmaceuticalmanufacturer.media)
This is the standard of decontamination that high containment labs require for areas hosting research on hazardous organisms. (amazonaws.com)

In the 1970s, the British Royal Air Force (RAF) was tasked with developing a portable isolation facility that could retrieve patients with infectious diseases. (cdc.gov)
The Trexler Air Transport Isolator, a portable isolation facility used to transfer patients with serious infectious diseases. (cdc.gov)
In the United Kingdom, 2 high-level isolation units (HLIU) are primarily responsible for the care of patients with viral hemorrhagic fevers (VHFs): the Royal Free Hospital, London, and the Royal Victoria Infirmary, Newcastle. (cdc.gov)
Both units use the Trexler patient isolator, in which patient care is provided within an isolation tent. (cdc.gov)
Comecer develops and manufactures high-technology systems for aseptic treatment and containment in the pharmaceutical and nuclear medicine industries, specialising in isolation technology solutions for regenerative medicine and tissue engineering. (pharmaceutical-tech.com)
Serving as an indispensable aid in meeting and overcoming these challenges are rapid transfer ports (RTPs), which were developed as a way to provide safe, contained transfer of sterile or hazardous materials and waste as they are moved into and out of containment or isolation. (medicaldesignbriefs.com)
The double-door transfer system allows all types of materials to be rapidly transferred into and out of cleanrooms, isolation chambers, or gloveboxes without breaking containment. (medicaldesignbriefs.com)

BioPharma Systems provides high quality technical and commercial support to North American clients and Global principal vendors across a variety of Pharmaceutical and Biotech arenas including: containment, aseptic processing, laminar flow/clean air technology, sterilization and filling systems. (cleanroomcompanydirectory.com)

You can create a secure aseptic processing workspace to prepare individual patient prescriptions while meeting the latest regulations, and protecting your patients and staff with the Bioquell Qube. (tecture.net)
Protect your staff, your patients, your prescriptions and your facility by using the Bioquell Qube and Hydrogen Peroxide Vapour technology. (amazonaws.com)

Vapor phase hydrogen peroxide technology reduces patient risk by decontamination of the areas where sterile doses are prepared. (thomasnet.com)
Bioquell offers a modular and unique containment system with built-in hydrogen peroxide vapor decontamination that can be used for non-sterile and sterile compounding, and can be vented for Hazardous Drugs (HDs) preparation utilizing negative pressure. (tecture.net)
Bioquell's options for the hospital pharmacy and drug compounding decontamination provide advanced Hydrogen Peroxide Vapor technology in your clean spaces and containment isolators. (tecture.net)
The rising pharmaceutical and biotechnology industries for various purposes by major industries, including vaccines, medical devices, API formulation or oncology studies, the growing incidence of hospital-acquired infections that require bio-decontamination continuously to provide patients with infectious agents' free environment, and the increasing outsourcing of bio-decontamination services is growing the bio-decontamination market. (datamintelligence.com)
An Evaluation of Environmental Decontamination With Hydrogen Peroxide Vapor for Reducing the Risk of Patient Acquisition of Multidrug-Resistant Organisms. (pharmamicroresources.com)

The companies said the system has been developed to allow transfer of sterile liquid through any type of walls that separate two areas with different levels of containment. (bioworld.com)
You can feel confident that your patients, staff and compounded drugs, whether sterile or non-sterile, are protected from contaminants. (tecture.net)
Comecer operates in the Radiophamraceutical sector through the production of shielding systems and equipment for special applications, in the Pharmaceutical field with the production of isolators for aseptic filling and / or dispensing systems for the treatment of sterile and toxic substances, and in the regenerative medicine sector for the handling, expansion and production of Advanced Therapies Products (ATMP) . (pharmaceutical-tech.com)
In some cases, barrier isolators intended for compounding sterile preparations are used either as an alternative or as an adjunct to traditional methods. (escolifesciences.us)
Isolator use for sterile compounding is relatively new to the United States. (escolifesciences.us)
Merck's manufacturing and sterility processes ensure the final integrated solution of the DPTE-BetaBag® and components - a sterile, single-use assembly that's ready to be integrated into an isolator filling machine. (getinge.com)

The following example presents a filter dryer discharge isolator with integrated pack-off feature, milling chamber and further PTS (Powder Transfer System) conveying to a second pack-off isolator with future extension for a micronising chamber installed on top of the existing enclosure, all of which meeting category OEB 5 (0.3 µm/m 3 , 8 hr TWA). (pharmaceuticalmanufacturer.media)
Unpacking, staging, storage, bag out/decon prep is done in the unclassified rightmost chamber called the Containment Vented Enclosure (CVE). (asepticenclosures.com)

These can be overpressure isolators if the main requirement is product protection, or negative pressure isolators if the user also needs to be protected against possible contamination from cell-damaging drugs of unknown toxicity. (carloerbareagents.de)
Most of these isolators are negative pressure. (escolifesciences.us)

Tightness can be verified with a test on the entire isolator, but the leak test on the entire chamber volume is not sensitive enough to find a microscopic leak in one of the gloves. (comecer.com)
Both isolators feature a Wash-In-Place (WIP) system consisting of hand-operated spray guns and additional spray balls in the upper chamber. (pharmaceuticalmanufacturer.media)
It draws air in from both the ambient and the middle chamber know as Containment Secondary Engineering Control. (asepticenclosures.com)

Both your life and the lives of your patients depend on the safety and performance of your barrier isolator. (airlabproducts.com)
Each ChemoSHIELD ® barrier isolator is made to order with details like seamless covered corners and single sheet construction to ensure a level of safety that is unparalleled in the industry. (airlabproducts.com)
The Baker SterilSHIELD ® Barrier Isolator offers a positive pressure work area for pharmacy applications. (airlabproducts.com)

There are 2 basic designs of Air Transport Isolator systems, closed and open, both of which offer maximum containment of highly infectious biologic agents. (cdc.gov)
1 µm/m 3 ) for which the industry increasingly uses isolators as appropriate containment systems. (pharmaceuticalmanufacturer.media)
Comecer began in Castel Bolognese, Italy when in the mid-1970s Carlo Zanelli founded Comecer SpA, a small company specializing in nuclear technologies that quickly grew to become a world leader in the field of containment systems for pharma, radiopharma and ATMP. (pharmaceutical-tech.com)
Our mission is to design and manufacture high-technology systems in the field of pharma, radiopharma and regenerative medicine , with the aim to continuously increase the accuracy and the safety of technicians, researchers, and patients. (pharmaceutical-tech.com)
Gazing into the crystal ball: how are containment systems evolving to meet future market challenges? (manufacturingchemist.com)
Bioquell's Dr Rolf Hansen examines how the latest isolator systems create aseptic working conditions, reduce risk and keep gene, cell and CAR-T the. (manufacturingchemist.com)
When combined with the industry trends of increased regulatory scrutiny and higher focus on patient safety, risk management, and compliance, the market is seeing an increased need for high-quality drug delivery systems such as prefillable syringes. (westpharma.com)
The design of production lines must be carefully considered, and reliable testing should be carried out to ensure that containment systems effectively minimise the potential for line operatives to come into contact with the materials. (cleanroomtechnology.com)
The equipment offered is from containment systems for operator and product protection thru materials handling devices and clean room architectural solutions. (cleanroomcompanydirectory.com)

This configurable isolator comes integrated with Bioquell's Hydrogen Peroxide Vapour technology. (tecture.net)
UV light and hydrogen peroxide share the following characteristics: (1) they cannot be used in an occupied space, (2) they are used after room cleaning to ensure maximum effectiveness, (3) they add to room turnover time, (4) they leave no harmful residue, and (5) they have no residual antimicrobial effect (i.e., they do not continue to kill microorganisms after a new patient is brought into the room). (pharmamicroresources.com)

This chapter describes practice and quality standards for handling hazardous drugs (HDs) to promote patient safety, worker safety, and environmental protection. (ihs.gov)
Health care workers who work with or near hazardous drugs may be exposed to these agents in the air or on work surfaces, clothing, medical equipment, or patient urine or feces. (escolifesciences.us)
Effective containment technologies are essential for limiting handler exposure to these hazardous compounds. (cleanroomtechnology.com)

Bioquell's solutions ensure your hospital pharmacy and compounding operations can retain their integrity while complying with the highest standards, ensuring your patients and staff are safe. (tecture.net)
Bioquell offers solutions to facilities opting to take charge of the compounding to maintain the drug's integrity as well as keeping your patients and staff safe. (tecture.net)
Partnering with customers to align drug packaging, containment, and delivery products with services, solutions and support. (westpharma.com)
This difficulty is compounded by the need for containment solutions to maintain operability and productivity while ensuring the safety of employees. (cleanroomtechnology.com)
Containment solutions including isolators and airflow protection. (cleanroomcompanydirectory.com)
Aseptic isolator processing solutions. (cleanroomcompanydirectory.com)
Aseptic Isolators by Tema Sinergie provides a comprehensive range of totally contained aseptic solutions , fully compliant with the strictest cGMP and international regulations , and can service the pharmaceutical, biological and hospital industries worldwide . (temasinergie.com)
Discover how flexible containment solutions, like ONFAB's isolators, can revolutionize the process and enhance the safety and quality of pharmaceutical products. (benchmarkproducts.com)
Dec designs customer-specific aseptic fill/finish solutions including the isolator system to house the process, if required. (dec-group.net)

We are committed to the highest standards of scientific excellence and integrity for the benefit of patients, the medical community, our partners, shareholders and employees. (innomedics.net)
Speedy Glove , the Automatic portable glove integrity tester: it is suitable for all isolators equipped with glove flange such as those dedicated to aseptic processes, containment processes, the manipulation of API and HAPI and the manipulation of radiopharmaceuticals. (comecer.com)
Isolator integrity is a must to ensure an aseptic workspace. (comecer.com)

We understand your need to move rapidly through clinical trial design and development to have built the capability to efficiently scale up drug product manufacturing processes to meet the demands of global clinical and patient supply requirements. (quotientsciences.com)
These types of containment technologies are effective in managing the risk of exposure from airborne dust particulates, as they are designed to improve containment for processes with a risk of airborne exposure, such as during all powder transfer stages. (cleanroomtechnology.com)
When integrated with isolators and other process equipment, SBVs enable material transfer while minimising the risk of material escaping before, during and after the transfer between two processes. (cleanroomtechnology.com)
This innovative mindset has revealed itself again with CRL's recent introduction of the new E Rapid Transfer Port, or ERTP (see the sidebar, "A New RTP Option"), which promises to make RTP operation easier than ever while maintaining the same product purity and containment capabilities that are the bedrock of life science production processes. (medicaldesignbriefs.com)
They provide their customers applications for containment, materials handling and aseptic processing technologies to increase yields and streamline processes. (cleanroomcompanydirectory.com)

The Bioquell SeQure provides a fixed solution with advanced controls to ensure critical areas can be quickly and easily decontaminated to the fullest extent, emphasizing patient and staff safety. (tecture.net)
This form of drug delivery system minimizes potential contamination from bacteria which further ensures patient safety. (pharmamanufacturingdirectory.com)
Settings in which antineoplastic HDs are prepared and administered will provide and maintain primary engineering controls, such as exhausted biological safety cabinets and compounding aseptic containment isolators, in conjunction with secondary engineering controls, such as buffer rooms or segregated compounding areas, consistent with U.S. Pharmacopeia (USP) chapters. (ons.org)
CARLO ERBA Reagents GmbH in Germany has specialized in the sale of isolators, microbiological safety workbenches, chemicals, personnel and material airlocks and other laboratory equipment . (carloerbareagents.de)
What do you see as trends in requirements in the area of containment for worker/product safety? (pharmtech.com)
Parenteral drug products, which include intravenous (IV), subcutaneous (SC), or intramuscular (IM) routes of administration, require careful planning, thoroughly trained personnel, and dedicated facilities to ensure patient safety. (quotientsciences.com)
Perhaps your comments can help provide clarity and enhance patient and staff safety! (asepticenclosures.com)
HDs must be handled under conditions that promote patient safety, worker safety, and environmental protection. (asepticenclosures.com)
While there is no doubt that this is an exciting time for the industry, and modernizations that help reduce costs, speed development, and increase product safety will ultimately benefit patients - a goal shared by all. (curiaglobal.com)
Exploring the use of next-generation containment technology as a means to comply with safety regulations and ensure the safest possible working environment for employees. (cleanroomtechnology.com)
To ensure safety and operability in the manufacturing process, pharmaceutical companies must carefully select appropriate equipment, outline procedures and utilise the right containment technologies. (cleanroomtechnology.com)
The industry requires cleanliness down to the molecular level to ensure drug purity and patient safety. (angstromtechnology.com)
Quality assurance, through microbial, particulate and pyrogen contamination control, is critical to ensure both drug and patient safety. (getinge.com)
Safety for staff and patients is the primary goal when handling and compounding drugs in the pharmacy. (nuaire.com)
Per US FDA's current good manufacturing practice (cGMP) guidance documents, a well-designed positive pressure isolator, supported by proper maintenance and monitoring, increase safety by preventing opportunities for microbial contamination during compounding. (nuaire.com)
The Exceeding Your Benchmark podcast interviews Jim Fries, the CEO of Rx360, a non-profit that works with pharmaceutical companies and their suppliers worldwide to protect patients from pharmaceutical-related safety issues. (benchmarkproducts.com)

CCMI is part of an established supply chain for ATMP products and has delivered several clinical programs aimed at offering patients alternative treatments through advanced therapies. (ispe.org)
The balance of sales derives from equipment for aseptic processing and packaging of specialised pharmaceutical products, as well as the production of isolating equipment and incubators used in Advanced Therapy Medicinal Products (ATMP) and regenerative cell therapies that use patient cells to grow new tissue. (pharmaceutical-tech.com)

The product also can make spinal fusion easier on patients by eliminating the traditional bone harvesting from a patient's hip, according to the company. (bioworld.com)
The level of containment required is determined by the pharmacological potency of the product to be handled. (pharmaceuticalmanufacturer.media)
In this isolator, the product passes through a milling unit (through-the-wall design) into a suction shoe from where it is transferred by means of a PTS into a pack-off isolator at a transfer distance of 8 to 10 m. (pharmaceuticalmanufacturer.media)
The need for flexibility in product development and manufacturing to support drugs for smaller patient populations seems to be increasing. (pharmtech.com)
ChargePoint Technology's Senior Product Manager, Ben Wylie, explores the latest trends in containment and advises how pharmaceutical companies can. (manufacturingchemist.com)
Curia, for example, has adopted multiple single-use disposables, including single-use glass, or ultralow-density polyethylene (uLDPE) formulation and filling vessels, pre-assembled, irradiated filters and filling lines, and single-use isolators for operator protection to minimize the potential for product contamination. (curiaglobal.com)
Moreover, many potential drug product applications involving HPAPIs can receive fast-track designation or accelerated approval, enabling the expedited delivery of new and effective treatments to patients with serious and life-threatening conditions. (cleanroomtechnology.com)
Potent manufacturing: Ensuring product containment is essential when working with toxic materials, not only for the operator, but for the surrounding environment. (medicaldesignbriefs.com)

The Trexler Air Transport Isolator (T-ATI) system has since undergone modifications and improvements. (cdc.gov)
Dedicated road transport that can accommodate the Air Transport Isolator patient transport system, such as the Jumbulance shown, enables seamless end-to-end transfer from patient pickup to the destination facility. (cdc.gov)
A single Trexler Air Transport Isolator patient transport system ready for use on a Boeing C-17 Globemaster transport aircraft. (cdc.gov)
Demarcation of clean and dirty zones during use of the Trexler Air Transportable Isolator patient transport system on a Boeing C-17 Globemaster transport aircraft. (cdc.gov)
Maintaining an effective containment system in a pharmaceutical environment where manual intervention is required can be particularly challenging. (cleanroomtechnology.com)
A streamlined interlock system with interchangeable three-bayonet and four-bayonet beta mount inserts that can be replaced without breaking containment. (medicaldesignbriefs.com)
You do not have to reposition the system and run several cycles or host multiple units whilst only lowering the amount of pathogens in a standard patient room. (amazonaws.com)
A single system can decontaminate every exposed surface of a standard patient room. (amazonaws.com)

In pharmaceutical and biologics manufacturing, a contamination event can lead to lost revenue, drug shortages for patients, and even a shutdown of your facility. (ecolab.com)
The DPTE-BetaBag® helps us to safely transfer our single-use filling components from outside an isolator to inside an isolator without the risk of contamination to the filling needles or the tubing. (getinge.com)

We are happy to offer you special isolators made of different materials such as stainless steel or plastic, which can be used in connection with bioreactors and other biotechnology devices. (carloerbareagents.de)

Both isolators are fabricated in accordance with cGMP standards featuring a fully welded design, ie the interior is constructed with rounded corners to provide smooth surfaces for easy cleaning. (pharmaceuticalmanufacturer.media)

Socket isolator offer compact, impact-rated design for heavy use in impact applications. (thomasnet.com)
There are numerous research applications that require clean air, particle containment, or both. (carloerbareagents.de)
The DPTE-BetaBag® is integrated into a single-use assembly designed for isolator liquid transfer applications and provided as a sterilized assembly. (getinge.com)

Dose calibrators designed to measure the radioactive patient doses to ensure the right dose is prepared for the right patient. (comecer.com)

Modular and podular laboratory and manufacturing allow rapid reconfiguration to support development of drugs for diverse patient populations. (pharmtech.com)

Use of less iodinated contrast is particularly crucial in patients with pre-existing renal dysfunction, as CM is concentrated in renal tubules, having a direct toxic effect, modulating tubular regulatory mechanisms, and producing renal vasoactive substances. (edu.au)

Currently, no UK-published guidelines exist on how to transfer such patients. (cdc.gov)

Take advantage of our state-of-the-art containment manufacturing for handling high-potency products, which features isolator technology and engineered controls. (quotientsciences.com)
U of T researchers develop liquid biopsy technology for prostate cancer Researchers at the University of Toronto have developed a new technology for a liquid biopsy to identify which patients might not respond to standard therapy for prostate cancer before it is. (cleanroomcompanydirectory.com)

Containment unit provides protection for pharmacy compounding personnel. (thomasnet.com)

MIC-EDU isolator Kill viruses, spores, fungi, mycobacterium and bacteria that may contaminate surfaces and cause diseases. (thomasnet.com)
This C-SEC is ISO5 used for wipe down type disinfection of all surfaces that are to be transferred into the Containment-Primary Engineering Control. (asepticenclosures.com)
Patients and healthcare workers can encounter a variety of infectious diseases that are easily spread throughout the facility from all surfaces including hard-to-clean contaminated equipment and high touch surfaces. (steramist.com)

Settings in which HDs are present will ensure that patients who receive these drugs and their caregivers receive education about safe handling to minimize unintended exposure in both the institutional and home settings. (ons.org)
For 2004] through primary prevention used to reduce exposure to hazard- patients, potential benefits of treatment measures such as engineering controls, ous drugs when other measures are not outweigh the risks from adverse side ef- administrative controls, and person- possible. (cdc.gov)

Since 2012, the DAIT, a joint Department of Health and Ministry of Defence asset, has successfully transferred 1 case-patient with Crimean-Congo hemorrhagic fever, 5 case-patients with Ebola virus disease, and 5 case-patients with high-risk Ebola virus exposure. (cdc.gov)
Since 2012, this team has successfully transferred 1 patient with advanced Crimean-Congo hemorrhagic fever ( 2 ) and 5 patients with Ebola virus disease (EVD) ( 3 - 5 ), 2 with recrudescence or late neurologic complications ( 6 , 7 ). (cdc.gov)

HD handling areas must be located away from breakrooms and refreshment areas for personnel, patients, or visitors to reduce risk of exposure. (asepticenclosures.com)

The C-PEC must be located in a C-SEC, which may either be an ISO Class 7 buffer room with an ISO Class 7 ante-room (preferred) or an unclassified containment segregated compounding area (C-SCA). (asepticenclosures.com)
We can place a room back into service faster, knowing it's safe for the next patient. (steramist.com)

End-to-end maximal patient containment from overseas to the receiving hospital and subsequent discharge is achieved through the T-ATI ( Figure 1 ), which is designed to interface with the Trexler isolator. (cdc.gov)

Chapter 2 is a retrospective study performed to determine the variability of major abdominal vessel and organ contrast enhancement and to establish any relationship with abdominal fat percentage in contrast enhanced CT studies, performed on 62 clinical patients at U-Vet Werribee Animal Hospital between February 2014 and February 2019. (edu.au)

Education, training, and competency evaluation will encompass the risks of exposure, including the reproductive and developmental effects, recommended precautions for specific handling activities, safe handling of contaminated patient excreta, proper disposal of contaminated waste, and handling acute exposure. (ons.org)
Our containment classification is based on the Performance-Based Level of Exposure Classification (PBLEC), allowing us to handle levels 1 through to 5 (or down to 0.1 µg/m 3 ) dependent upon the type of compound, dosage form, and batch size. (quotientsciences.com)

An individualized plan of progressive exercise initiated as soon as possible in the recovery process is the best way to ensure the total recovery of the patient in the least amount of time and with fewest complications (4). (forex-consultant.com)

Download the clean air and containment decision map and make your decision easy. (rapidmicrobiology.com)

As one of the most comfortable isolators in the industry, the ChemoSHIELD ® features a slanted viewscreen with a top hinge that allows for full opening for loading and unloading of pharmacy instrumentation or equipment. (airlabproducts.com)

This guide is intended to provide an overview of isolators and assist individuals considering their use in purchasing, installation and commissioning issues. (escolifesciences.us)
With over 300,000 decontaminations under our belt, supported by a large library of independent peer-reviewed scientific literature, Bioquell's services and equipment are designed to eliminate doubt and provide you and your patients with the safest environment. (amazonaws.com)

Infuse Bone Graft/LT-Cage allows Australian spinal surgery patients access to a treatment that eliminates painful bone graft harvesting [while] at the same time creating a fusion," said Dr. Peter McCombe of St. Andrew's War Memorial Hospital (Brisbane, Australia). (bioworld.com)
For many years we have been distributing isolators for the hospital pharmacy , in which medicines are mixed and prepared for the patients. (carloerbareagents.de)
The United Kingdom is unique in that probably 90% of all cytotoxic reconstitutions in hospital pharmacies are now carried out in isolators. (escolifesciences.us)

Chances are the biopharmaceuticals prescribed for your patients or even the flu shots given have been made in an area protected by Bioquell. (amazonaws.com)

40 years, the British Royal Air Force has maintained an aeromedical evacuation facility, the Deployable Air Isolator Team (DAIT), to transport patients with possible or confirmed highly infectious diseases to the United Kingdom. (cdc.gov)

For these activities we offer special isolators with a controlled atmosphere. (carloerbareagents.de)

Their aim has been to reduce the number of persons handling antineoplastic agents, thus diminishing the risks for themselves, the nursing staff and the patients. (escolifesciences.us)

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