About
Leaders in Regulatory Affairs for the Medical Device Industry
PaxMed is a regulatory and clinical trials consulting firm specializing in services to manufacturers of implantable medical devices. These services include regulatory strategy; submissions to FDA and international regulatory bodies; design and management of clinical trials (strategy, protocol development, CRFs, monitoring, data management, biostatistics and reporting); and development and implementation of quality systems. Biomaterials specialties include ceramics, metals, bioabsorbable polymers...
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Detailed Information
- Location TypeSingle Location
- Opening Date1990
- Annual Revenue Estimate$1 to 2.5 million
- SIC Code show
- Employees5 to 9
- Contactsshow
- Founder / President Floyd Larson
- Senior Quality Systems Specialist Ellen Esterline
- Vice President and Director of Regulatory Affairs Kevin Thomas
- Senior Clinical / Regulatory Specialist Linda Schulz
- Manager of Business Administration Carolyn Poirier
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