The global medical device landscape is complex. Getting a new product or therapy approved requires compelling clinical evidence. At NAMSA, we know what you’re up against and understand how to set you up for success.
With a dedicated focus on medical device and IVD products, we’ve designed and conducted trials in every area of the world to address wide-ranging client objectives—from first-in-human through post-market.
We partner with you to work smart from the start, saving you time and preventing costly do-overs. Our clinical experience encompasses a broad range of technologies, therapies and global markets.
Our clinical expertise spans every manner of technology, therapy, indication and geography. This broad range of experience allows us to successfully lead our clients through all phases of clinical research: from first-in-human to pivotal and post-market. NAMSA’s global footprint provides clients direct access to local networks to conduct safe, effective and efficient clinical trials, which are optimized to achieve regulatory approval and continued innovation.
Access our Clinical Research Services Brochure by selecting “Download PDF” on the left.