Medical Device Testing Services In USA
-
based in 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 ...
-
based in USA
When materials are to be implanted in patients, quality is of the utmost importance. Failure to meet the rigorous standards of medical device OEMs can have devastating results for patients and their families. Ensuring your materials are made to your specifications and investigating failures promptly and accurately are both critical to ...
-
based in 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 ...
-
based in USA
Anresco Laboratories now offers medical device testing services to assess the conformity of personal protective equipment (PPE) to required specifications. Services offered ...
-
by Inotivbased in 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 ...
-
by STEMartbased in USA
An active implantable medical device (AIMD) is any active medical device that is intended to be totally or partially introduced, surgically or medically, into the human body or by medical intervention into a natural orifice for diagnostic or therapeutic purposes, and which is intended to remain ...
-
based in 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 ...
-
by STEMartbased in 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 ...
-
by STEMartbased in 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 Curiabased in USA
As an independent, third-party laboratory, we are a trusted testing partner for distribution testing, packaging materials qualification and product testing. We provide technical expertise, market-leading technology and customized solutions for your unique needs. Our experts can help you better understand testing requirements, ...
-
Manufactured by Sanbor Medicalbased in 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. ...
-
Manufactured by DemeTECH Corporationbased in 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 ...
-
based in 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 ...
-
by STEMartbased in 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 ...
-
by Inotivbased in 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 ...
-
Manufactured by MediPurposebased in 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 ...
-
Manufactured by Ceutical Labsbased in 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 ...
-
based in 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. ...
-
based in 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 ...
Need help finding the right suppliers? Try XPRT Sourcing. Let the XPRTs do the work for you