Global MedTech product launches depend on more than registration speed—they require predictable cycles, first-time submission accuracy, and efficient parallel country filings. Success hinges on systems with embedded market intelligence to capture regulatory variations and share insights globally. IQVIA’s registration framework automates transactional tasks while enhancing regulatory work, improving clarity in launch planning. Challenges include safety-driven reclassifications, political factors like Brexit, and varied country requirements that demand extra testing or localized data, making launches longer and costlier without connected intelligence and purposeful design.

Join for free to read