Priority Designs brings over 25 years of product development experience to the medical device industry. Our full-service capabilities span the entire medical product development process, from initial human factors and usability, to design and development, to verification and validation.
The medical design team includes biomedical engineering, human factors and usability researchers, designers, soft goods experts, and prototyping specialists. Our pragmatic approach to product development assures your product meets the needs of the users, development team, and ultimately, the FDA.
Continuous improvement has been a cornerstone of Priority’s success over the past 25 years, allowing us to grow our capabilities to meet our clients evolving needs. Achieving ISO 13485 certification for contract conceptual design and development of medical devices furthers our commitment to meet the quality and regulatory requirements critical to the success of our medical device partners.
As every client engagement is unique, our quality system was designed to be tailorable to the specific needs of each project. This allows our development teams to remain nimble and responsive, while assuring the appropriate level of rigor can be applied when required.
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At Priority Designs, our medical device development pulls in experts across the whole product development process including:
- Soft Goods
While many projects are in development or under FDA review, we aren’t able to show many details, but our medical device specialists have worked across a variety of medical projects including the topics shown here.