Published on March 11, 2014
Regulatory Consulting ► Regulatory ► Quality System (QSR) & ISO ► Product Safety & Validation ► Clinical & Statistical ► On-Site Support ► Consulting ► International Registrations ► US Agent 2
R&D Support ► Material Characterization & Analytical Chemistry ► Efficacy and Functional Studies ► Histopathology Services ► Biological Safety Evaluation Plans ► Product & Process Risk Assessment ► Shelf-life & Accelerated Aging Studies ► Cleaning Studies ► Method Development and Validation Services ► Particulate Analysis ► Human Anatomic Services ► Physician Training 3
Non-Clinical ► Biocompatibility ► Histopathology 4
Clinical Research ► Biostatistics ► Study Design ► Study Management ► Field Clinical Engineers ► Data Management/EDC ► Data Safety/Clinical Events ► Report & Manuscript Writing ► Clinical Evidence/Post Approval ► Clinical Auditing 5
Post-Market Support ► Sterilization Validation ► Environmental Monitoring ► Packaging Validation & Shelf Life Testing ► Reusable Device Studies ► Other Microbiology Testing Services ► Sterilization Monitoring Products 6
► For more information on NAMSA services ► Visit NAMSA Services ► For more information on testing or to request a quote ► Contact us at email@example.com 7
Provides biological, chemical and physical testing services to the medical device industry, and offers education, consultation and on-site evaluation of ...
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NAMSA’s balance of trusted advisors and proven process lets us support clients across the entire medical device product development spectrum.
NAMSA has over 45 years of providing expert regulatory, laboratory, clinical, and compliance services as a Contract Research Organization (CRO)
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Primarily serving the health care industry, NAMSA offer testing services to medical device manufacturers, raw material suppliers, pharmaceutical companies ...
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The clinical research can be the most expensive and time consuming. NAMSA's expertise can help prevent those costly do overs.