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Preclinical GLP Research Studies for Medical Devices
Experience Matters. Why Companies Choose NAMSA.
Medical Device GLP Preclinical Projects Last 12 Months
Labs in US and Europe Offering Preclinical Ô°ÇøÒùÂÒ
Fully Equipped ORs and Cath Labs in US and Europe
Of All Successful FDA PMAs Last Year Were Supported by NAMSA
GLP Studies in a Wide Variety of Therapeutic Areas and Models
The Ô°ÇøÒùÂÒteam has extensive experience conducting GLP-compliant studies on a vast array of medical devices in the following areas:
- Cardiovascular*
- Dental
- Diabetes care
- Gastroenterology*
- General surgery*
- Neurovascular*
- Ophthalmology
- Orthopedics*
- Peripheral vascular*
- Wound care*
*Extensive expertise in this area
Full Compliance with Good Laboratory Practices (GLP)
We understand the criticality of complying with methods and regulations within the European Committee for Standardization (CEN), U.S. Food and Drug Administration (FDA) and other international guidelines to provide reliable, accurate outcomes.
Do We Have Expertise With Your Device?
Want to learn more about our GLP preclinical experience for your specific category of device?
Ô°ÇøÒùÂÒLab Equipment and Facilities
Ô°ÇøÒùÂÒoffers cutting-edge equipment and techniques. We have numerous digital catheterization labs featuring state-of-the-art Fixed C-arm platforms. We can accommodate your timelines no matter how large the study design or last minute the request. Each cath lab features dedicated workstations for real-time quantitative analysis and evaluation. See a comprehensive list of equipment here.
Meet Our Preclinical Experts
Explore the depth of our team’s expertise.
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Jack Risdahl, DVM, PhD
Principal Strategy Consultant, PreclinicalView Bio -
Gaëlle Clermont, PharmD, PhD
Principal Strategy ConsultantView Bio -
Michael A. Jorgenson, BS
Principal InterventionalistView Bio -
Tyler LaMont
Senior InterventionalistView Bio -
David Reimer, MD
SurgeonView Bio -
Corey Leet
Director, Regional Preclinical and In-Vivo Biocompatibility OperationsView Bio