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Deep Preclinical and Clinical Expertise in Numerous Categories
NAMSA has worked with tens of thousands of devices since 1967 but we have developed particular expertise in the device categories shown below.
All Services
Need to Get It Right the First Time? Look to NAMSA.
Every year more than 3,000 medical devices and In Vitro Diagnostic companies worldwide trust NAMSA to help them bring innovative new products to market or ensure the ongoing safety of their existing products. Our team of 1,400 specialists are ready to help you conduct market research, preclinical studies, clinical trials, biological safety testing, regulatory submissions, and much more.
Explore Our Services
From startups to multinationals, NAMSA has been serving the medical device and IVD industries since 1967 and has a highly experienced team ready to serve you.
Consulting & Strategy
Assistance with biological evaluation plans and reports, FDA, EU MDR and IVDR submissions, market research, post-market compliance, and more.
Preclinical Research
Unparalleled preclinical laboratory support for sponsors at GLP-compliant and AAALAC-accredited facilities in the United States and Europe.
Clinical Research
Extensive medical device and IVD clinical trial expertise spanning all stages of clinical research. Global footprint provides clients direct access to local networks.
Medical Device Testing
State-of-the-art labs conduct 118,000+ biocompatibility, microbiology, sterility and other tests annually. No other company conducts more tests.
Meet NAMSA’s Team of Experts
NAMSA has built a reputation for excellence based on the deep industry expertise and client service offered by our team. Meet the consultants, scientists, medical writers, toxicologists, biostatisticians, surgeons and other experts who make NAMSA the preferred choice of device and IVD companies worldwide.
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Adam Saltman, PhD, MD
Principal Strategy Consultant, Clinical and Regulatory ServicesView Bio -
Wendy Schroeder, BSN, CCRC/PM, CRCP
Principal Strategy Consultant, ClinicalView Bio -
Pedro Eerdmans, MD, PhD
Director, Global Strategy ServicesView Bio -
Corie Diaz, BA, MBA
Global Director, Clinical OperationsView Bio -
Kenneth Ouriel, MD, MBA
Chief Medical OfficerView Bio -
Gaëlle Clermont, PharmD, PhD
Principal Strategy ConsultantView Bio
Supporting All Phases of the Medical Device Development Lifecycle
We work with a wide range of medical device and IVD manufacturers, from startups developing their first device to multinational companies with thousands of SKUs. No matter what your need is, our highly refined internal processes allow us to efficiently handle everything from routine medical device testing to long-term clinical trials.
Why Clients Choose NAMSA
From preclinical testing, clinical trial management and regulatory strategy, NAMSA is truly expert at delivering high quality outcomes throughout the entire medical device development continuum. Start to finish, NAMSA understood the required activities for accelerated development and efficacious market introduction.
Shawn Shorrock, Former Global Director, Solvay Dental 360
3,000
Medical Device Clients Served Each Year
270
Medical Device Clinical Projects Last Year
118,000
Medical Device Tests Conducted Last Year
6
Global Lab Locations Doing Device Testing
