Regulatory and Quality Consulting
Having the right regulatory partner at the right time can be invaluable in attaining compliance and market access. NAMSA provides a wide-range of regulatory services across the full spectrum of product design and development through post-market support. From Notified Body selection and Pre-IDE preparation to Advisory Panel Meetings, our experts develop and implement global regulatory strategies to accelerate your specific commercialization efforts—ultimately getting you to market faster so you may make a more immediate impact on patient safety and healthcare. Services: Regulatory Assessment, Compliance and Strategic Support, Post Market Support, Medical Writing, Quality Systems & Compliance, Biological Safety & Validation Consulting; FDA U.S. Agent Services; International Medical Device Registration Consulting.