Navigate global markets — Insight into convergence and reliance, regulating advanced therapies & adhering to data requirements
Streamline your global regulatory submissions and seamlessly break into new regions including APAC, MENA, LATAM and beyond
Deep-dive into the global requirements of pharmaceuticals with Iraqi Ministry of Health, Saudi FDA, EARAPA, Astra Zeneca, Sandoz and more
Uniting regulatory authorities, trade associations and industry professionals from around the world
Propel global harmonisation and accelerate development to market timeline
Compare and contrast global reliance through our multi-stakeholder panel
Identify regional initiatives in APAC, MENA and LATAM to accelerate product acceptance
Apply industry learnings from AstraZeneca, Sandoz and GSK
Understand the complexities of regulating global advanced therapies (ATMPs)
Understand the current global landscape of regulating ATMPs
Curate compliance strategies to ensure product approval across APAC, LATAM and MENA
Take advantage of lessons learned in regulating ATMPs through panels
Benefit from first-hand experiences on utilising real-world evidence (RWE)
Decode the regulations of sufficient data and RWE across the globe
Enhance your data collection approach through in-depth, regional case studies
Prepare for the future of data collection and submission with our forward-thinking panel
