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Sterile Scope Testing Services In Usa
10 services found
by:Environmental Tectonics Corporation (ETC) based inSouthampton, PENNSYLVANIA (USA)
ETC’s Field Service Network operates out of offices worldwide and provides service & support for all Sterilizers. Our Field Service Engineers are professionals who spend time working in our manufacturing areas building & testing sterilizers. After sales service & support provided by ETC include: equipment rigging, installation, start-up, site acceptance testing, validation ...
Manufactured by:Innovative Health LLC based inScottsdale, ARIZONA (USA)
Reprocessing means collecting used single-use medical devices, shipping them to a regulated reprocessor, and buying them back at about half the price of a new device, to reduce supply costs without adding risk. After a procedure, single-use devices are wiped down and sometimes flushed, then collected from the hospital and shipped to the reprocessor. Here, they are sorted and identified to ensure ...
Manufactured by:ARMI - Advanced Regenerative Manufacturing Institute based inManchester, NEW HAMPSHIRE (USA)
We offer regulatory consulting services to support our member organizations with preclinical study design, FDA submissions and interactions and clinical trial design to support existing industries and grow new ones. ...
Manufactured by:Plastic Ingenuity based inCross Plains, WISCONSIN (USA)
Being the best custom thermoformer means having strong capabilities that are matched to the markets we serve. Our in-house structure, coupled with our deep industry expertise and wide geographic footprint, allows us to be the one-stop-shop for all your thermoforming ...
Manufactured by:Assured Bio Labs, LLC based inOak Ridge, TENNESSEE (USA)
Assured Bio provides assistance in complying with the environmental sampling requirements addressed in U.S. Pharmacopeia (USP)Pharmaceutical Compounding—Sterile Preparations. USPapplies to health care institutions, pharmacies, physicians practice facilities, and other facilities in which compound sterile preparations (CSP) are prepared, stored, and dispensed. It provides the practice ...
Manufactured by:Noxilizer, Inc based inHanover, MARYLAND (USA)
Noxilizer’s expert in-house microbiology and materials science team will work with you to perform sterilization testing to your requirements. We offer a wide range of testing services that conforms with ISO standards both in-house at our Hanover, MD facility and through external labs. Each customer has a dedicated team working through every step of the ...
Manufactured by:Ceutical Labs based inFlower Mound, TEXAS (USA)
There are several distinct markets that are served by the Analytical Testing Division. They include Pharmaceutical, Nutraceutical, Medical Device, API (Active Pharmaceutical Ingredient), NDI (New Dietary Ingredient) and Post Sterilization Testing. Two of these categories, API and NDI require additional explanation. Their definitions are as follows: API -An API is an active pharmaceutical ...
Manufactured by:Minaris Regenerative Medicine, LLC based inAllendale, NEW JERSEY (USA)
Minaris Regenerative Medicine’s manufacturing development services help you to design efficient and robust manufacturing processes for your cell and gene therapy. Keeping the ultimate goal of commercial supply in mind, we help you think beyond your current manufacturing needs to create approaches that improve the commercial viability of your products. We keep in mind four key elements of ...
by:Life Science Outsourcing, Inc. based inBrea, CALIFORNIA (USA)
The medical device packaging design, testing, and validation process can be intricate and time-consuming, facing intense regulatory scrutiny and often being the largest cause of FDA recalls. Starting medical device packaging validation too late in the design process can create significant challenges for most new product launches. Life Science Outsourcing is a medical device contract ...
by:TÜV SÜD America Inc. based inWakefield, MASSACHUSETTS (USA)
In the medical field, practitioners utilize a range of devices to address patient health, from diagnosis to surgery. When the patient comes into contact with a medical device or material, it should fulfill its intended function without harming the patient. Therefore, all medical devices need to undergo a thorough biological risk assessment to protect the patient from any toxic, physiological, ...