The Abrimed team includes regulatory compliance consultants, engineers and healthcare professionals. We serve many segments of the healthcare industry with emphasis on medical devices, pharmaceuticals, biotechnology, clinical diagnostics and dietary supplements. We also serve general industrial clients with ISO regulatory compliance and certification. Our regulatory process services address each phase of a product’s life cycle from conception, through design, development, clinical trials, regulatory approvals, market introduction, sales, distribution, manufacturing and ongoing management. We offer a wide range of services throughout each phase.
Based in California, we assist domestic firms throughout the US, as well as international clients mainly in Europe and Asia (China). We work with government agencies, public and private research institutes, laboratories and industry. Learn more by exploring the following links, or Contact Us to discuss your specific needs:
