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Medical Device For Cognitive Assessment Testing Services In Usa
21 services found
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: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 ...
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: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 ...
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 ...
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: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: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: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 ...
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 ...
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: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: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. ...
by:Anresco Laboratories based inSan Francisco, CALIFORNIA (USA)
Anresco Laboratories now offers medical device testing services to assess the conformity of personal protective equipment (PPE) to required specifications. Services offered ...
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, ...
by:North American Science Associates Inc.(NAMSA ) based inNorthwood, OHIO (USA)
If your device doesn’t perform according to its intended function, your agenda can be turned upside down. So when you’re looking for an accelerated path to market, you want a partner who offers a broad range of in vivo models and analytical tools that will provide you the data you need to support the specific application of your ...
by:Inotiv based inWest Lafayette, INDIANA (USA)
We provide GLP and non-GLP nonclinical testing for the pharmaceutical and medical device industries. Our focus on superior service, advanced animal care, and ongoing commitment to excellence ensure your study’s success. We have multiple surgical suites, a team of trained veterinary surgeons, and state-of-the-art imaging ...