Preclinical and Clinical Research, Regulatory Consulting, Biocompatibility Testing, PRODUCT DEVELOPMENT STRATEGY, MEDICAL DEVICE TESTING, CONTROLLED ENVIRONMENTAL REGULATORY TESTING SERVICES, BIOLOGICAL SAFETY CONSULTING, CLINICAL RESEARCH, PRECLINICAL RESEARCH, MEDICAL DEVICE REGULATORY & QUALITY, MEDICAL WRITING SOLUTIONS, MEDICAL DEVICE REIMBURSEMENT, IVD, NAMSA APEX PROGRAM™, MEDTECH MARKET RESEARCH CONSULTING, Bioskills Cadaver and Simulation Labs, Imaging and Data Collection Modalities, Interventional and Surgical Research, Non-GLP Preclinical Surgical Research, Pharmacology and Toxicology, Pathology, Usability Testing, High Resolution radiography (Faxitron), Histomorphometry, Scanning Electron Microscope, Stereomicroscopy, Post-Mortem Exams, Large / Small in vivo models, Evans blue staining, Ex-vivo perfusion fixation, Fluorogram guided tissue harvesting, In-situ perfusion fixation, Microdissection, Pharmacokinetic sampling, TTC in-situ and ex-vivo staining,
Brief Description:Â
NAMSA is a global CRO specializing in medical device testing and development, offering services to support preclinical and clinical research, as well as regulatory affairs for medical devices.
We will review the reports from both consultant and Client to give the best decision. It will take 3-5 business days for reviewing after receiving two reports.