Exova has a proud history supporting customers to introduce new patented products and processes to the dynamic medical device market. With a clear understanding of your markets, regulations, and challenges, we provide our expertise and experience with cGMP, GLP, ISO/IEC 17025 testing to help your product reach the market sooner and with safety and quality built in.
Our engineers and scientists work closely with customers to support them at every stage of their product lifecycle, from initial concept development to prototype manufacturing, process and release test method development and implementation.
Understanding the urgency of compressing product development cycle time helps to get your product to market faster. Your intellectual property is secure, and any test methods or technology we develop remains within your ownership. And, of course, we understand the commercial demands on your time, so flexibility and efficiency are by-words for Exova.
Our analytical development chemists complete our team, ensuring that all work is supported by the best available analytical data. These end-to-end skills and capabilities ensure we can not only meet your technical needs but also help to reduce your product development cycle-time and improve the speed of innovation.
We offer a full range of medical device testing, including:
- Medical device prototype design
- Materials selection
- Product and process development/combination products development
- Equipment design and medical device fabrication
- Custom polymer synthesis
- Failure analysis
- Regulation/equivalency testing
Contact UsWhatever your query, we'll pass it on to our experts and respond within a very short space of time.More details
1300 First State Blvd, Suite C,
Wilmington, DE 19804
Contact: Waheed Sheikh - President
Tel: +1 302-636-0202
Fax: +1 302-636-0204