Southern California’s Proven Leader in Bringing New Medical Device Innovations from Concept to Commercialization
|For nearly two decades, U.S. and internationally-based medical device companies have relied upon Southern California’s DeviceLab’s guidance to swiftly and effectively move their clinical innovations through the medical design and development process.
Anybody that’s been through the process knows that new medical device design and development outcomes can be expensive and time-consuming. However, because DeviceLab continues to refine—and many cases, redefine—best practices for steering Class 1, 2 and 3 medical devices “from concept to commercialization,” your new medical device can get to market with efficiency and economy. This is particularly crucial when needing to get approval from regulatory organizations such as the U.S. FDA.
How do we do it? First, we have ISO certification for medical device development, which validates that we adhere to the highest standards for quality management systems (QMS). This certification is regularly audited to ensure that we continue to maintain our medical device design and development QMS.
Second, we have the best and brightest medical device designers and developers at our disposal. From our highly-skilled employees to our extensive network of consultants, contractors and partners, our qualifications and capabilities enable us to expertly address all aspects of your new medical device’s design and development.
We invite you to learn more about many successful medical device design and development projects, or if your company is ready to start taking its innovations from concept to commercialization, contact us today!