STEMart Introduces Medical Device Testing Services for Research Community

STEMart introduces medical device testing services for researchers all over the world.

New York, USA – March 1, 2021 – As a provider of integrated medical device CRO services dedicated to medical device and diagnostic clinical development, STEMart recently introduces medical device testing services for researchers all over the world. In accordance with ISO 10992 and ISO 18562 standards, FDA guidance, ASTM (American Society of Testing Materials) standards and other international guidelines, STEMart’s experts with years of experience in a variety of testing services for Class, I, II and III medical devices now can provide assistance for clients to ensure that every aspect of medical device is properly inspected.

As medical devices are subject to risk, comprehensive medical device testing throughout the entire product life cycle is a critical step in the transformation process from an innovative design into a reliable and marketable product. STEMart now offers medical device testing services such as biocompatibility testing, microbiology & sterility, packaging solutions, facility & process validation, physical testing service, and preclinical medical device testing service for customers choice.

STEMart specializes in all kinds of fields including urology, neurology, dental, cardiovascular, ophthalmology, and imaging. It applies professional services throughout extensive experience conducting medical device clinical studies across multiple therapeutic areas to researchers’ studies. Its medical expert services range from medical device design, prototyping, pilot production, testing, medical device certification services to the manufacturing processes.

“Combining expert medical product testing knowledge with the state-of-the-art laboratories and facilities, STEMart provides a one-stop, client-specific approach for testing of both active medical devices, non-active medical devices and In Vitro Diagnostic equipment. For instance, we can help manufacturers conduct a variety of In Vitro and In Vivo safety evaluation studies according to ISO 10993 and ISO 18562 standards on medical device to identify the presence of toxins or any other potentially harmful effects.” said Tina Frederick, Executive Director of Marketing at STEMart.

“We’re glad that we are able to bring comprehensive medical device testing services to scientific communities, and having this resource available within our facility will allow us to provide more professional services to our global clients. We can provide expert services to help medical device manufacturer validate terminal sterilization processes, and evaluate methods for cleaning and reprocessing reusable devices and instruments. We believe such newly offerings will advance our clients’ important studies.” said Brian N. Griffith, Product Portfolio Manager at STEMart.

If you want to know more details on medical device testing services or would like to consult with the experts at STEMart, please contact STEMart directly, or visit STEMart at

About STEMart

STEMart is an industry-leading eCommerce platform with an expanded global footprint and has a broad portfolio of more than 10,000 products. It aims to provide best-in-class lab materials, medical instruments and consumables, excellent technologies, and high-quality services to global customers in the fields of science, technology, and engineering, from the discovery stage towards the manufacturing process. STEMart is dedicated to making research and biotech production simpler and safer, and through that to accelerate access to better health for people everywhere.

Media Contact
Company Name: STEMart
Contact Person: Staci Horne
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Phone: 1-631-619-7922
Country: United States