FDA Regulatory Roadmap - Drop-in Clinic offers UK and European life sciences and medical device companies personalised, 1-on-1 consultations with FDA specialist Mark Swanson. The 20-30 minute sessions will provide tailored guidance on navigating U.S. FDA regulations.

This consultation offers an opportunity for businesses to develop a customised roadmap for FDA clearance/approval, optimise their regulatory strategy and quality management systems, and receive expert advice on product approvals, labelling, cGMPs, and other regulatory challenges.

Mark Swanson, a regulatory expert with over 25 years of experience, has helped numerous UK and European companies succeed in the U.S. market, making this an invaluable opportunity for businesses aiming for FDA compliance and market entry. Limited slots are available, so early registration is encouraged.