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Medical Device For Cognitive Assessment Testing Services Available In Usa
28 services found
Manufactured by:SRT-Microcéramique based inVENDOME, FRANCE
Burn-in testing is a service designed to identify any potential defects in electronic components before they are dispatched to customers. This testing process subjects the components to thermal cycling and power cycling to simulate extreme operational conditions. The primary goal is to catch weak components that could fail prematurely during normal use, which could impact the reliability of the ...
Manufactured by:DemeTECH Corporation based inMiami Lakes, FLORIDA (USA)
DemeTech’ s R&D Department will design, develop, prototype medical device ideas. After testing and proof of concept, we can develop final production models and provide scalability for mass ...
by:STEMart based inShirley, CALIFORNIA (USA)
Processes close or equal to those to be used in production. Pilot production is a crucial process for devices that will be tested in clinical trials or pilot markets before transitioning to full-scale production. If the customer’s medical device is successful in a pilot market or clinical trial, it will likely transition to full- scale production. But if the medical device has flaws that ...
Manufactured by:Sanbor Medical based inAllentown, PENNSYLVANIA (USA)
Sanbor Medical offers a full range of medical device testing and programming capabilities to help our customers delight their users and succeed long-term. ...
by:Protheragen-ING based inNEW YORK (USA)
The safety and effectiveness of medical devices are of paramount importance in the healthcare industry. Before these devices are approved for use, they must undergo rigorous testing to ensure that they meet the necessary safety standards. Protheragen-ING Lab specializes in providing comprehensive and reliable medical device safety testing services. Our state-of-the-art facilities, experienced ...
by:Emmace Consulting AB based inLund, SWEDEN
Testing and determination of Particulate Matter (PM) and Volatile Organic Substances (VOS) according to ISO 18562-2 and ISO ...
by:IMR Test Labs based in
Our Mechanical Fatigue Testing Services Laboratories utilize cyclic loading (HCF-LCF) to predict the life of materials under fluctuating loads and temperatures. Determining fatigue life can support research and development efforts for new materials as well as prevent failures and recalls when used to ensure material properties. Understanding a material fatigue life is critical in the markets we ...
by:Proregulations based inSanta Clara, CALIFORNIA (USA)
Medical device packaging testing is to verify and test the performance of packaging in a laboratory. Registration data for medical and medical products are required to include the results of packaging studies to demonstrate the safety and effectiveness of the contents after delivery, transportation, storage and until ...
Manufactured by:MediPurpose based inDuluth, GEORGIA (US) (USA)
The MediPurpose™ Medical Device Innovation division collaborates with medical device inventors and innovators to take new medical devices from concept to commercialization—bringing together financing, proven medical device development methodology and global experience to help ensure success. Taking a new medical invention from concept to commercialization can be a difficult process, ...
by:Inotiv based inWest Lafayette, INDIANA (USA)
You’ve worked hard to get this far. Rely on Inotiv’s scientific leadership and attentive, decisive advice to uncover potential flaws in your novel pharmaceutical compound that might limit its development — before you invest significant time and ...
by:Emmace Consulting AB based inLund, SWEDEN
ISO 18562-4 addresses the critical need for quantifying and assessing the risks associated with condensate produced during patient use, which can potentially enter the lungs or the throat region depending on the device. Accurate measurement of the condensate volume is essential for ensuring patient safety, meeting regulatory requirements and making it possible to estimate the exposure to ...
by:Protheragen-ING based inNEW YORK (USA)
Reusable medical devices, such as surgical instruments, endoscopes, and anesthesia equipment, offer a cost-effective and environmentally friendly alternative to disposable devices. However, the complexity of these devices, coupled with the potential for biofilm formation and residual contamination, presents unique challenges in ensuring their safety and effectiveness. Protheragen-ING Lab ...
by:Microbac Laboratories, Inc. based inPittsburgh, PENNSYLVANIA (USA)
Microbac understands the new challenges facing biomedical companies as the industry undergoes rapid change and the introduction of radical new device designs, biomaterials, and testing techniques. Our staff focuses on working with you to develop a medic device testing regime that will assist in turning your prototype products into the innovations of tomorrow. Mechanical medical device testing is ...
by:Product Safety Consulting, Inc. based inBensenville, ILLINOIS (USA)
Careful attention to product compliance and certification are an integral part of the process of developing and marketing medical devices. Certifiers, regulators,and standards-writing bodies such as Underwriters Laboratories (UL), the Canadian Standards Authority, the IEC and the FDA have been working hard to keep up with the pace of change in biotechnology — which has led to a dynamic and ...
by:Test Labs Ltd based inPeterborough, UNITED KINGDOM
Test Labs Ltd provides comprehensive accelerated and real-time aging testing services to evaluate the stability of products under various storage and use conditions. Accelerated aging testing simulates long-term aging processes by exposing products to elevated stress conditions, such as increased temperature and humidity, over a shorter period. This method allows for fast evaluation of shelf-life ...
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:Bastos Viegas, SA based inGuilhufe, PORTUGAL
Bastos Viegas SA always had and still has as one of its main objectives produce high quality and meeting the requirements of its customers and the market in general as well as all applicable legal requirements. Therefore Bastos Viegas bet on the implementation and constant updating of a quality control system that currently has decades of experience. In this sense always equipped its laboratories ...
by:ALS Environmental based inHouston, TEXAS (USA)
At ALS our Pharmaceutical Division is a provider of testing services to the Pharmaceutical and Healthcare industries in Australia, Europe and Asia. Committed to exceeding customer expectations we are able to provide high quality solutions across a range products, including human and veterinary products, intermediates and raw materials. Testing is conducted according to international standards ...
by:STEMart based inShirley, CALIFORNIA (USA)
STEMart performs a variety of testing for partial and total hip joint prostheses to measure how they will withstand different levels of fatigue, compression, torsion, and bending over an extended period of time. ...
by:STEMart based inShirley, CALIFORNIA (USA)
Cytotoxicity testing is a sensitive method to assess the biocompatibility of a material extracted through a specific cell culture media following exposure of the extracted fluid to L929 cells. This test is performed on raw materials in the manufacturing process, all medical devices contacting patients, and devices undergoing a sterilization validation. ...