Global Regulatory Affairs: Key Activities and Emerging Trends

We are excited to welcome Sanjiv Verma as a speaker at Zurich Life Science Day 2025!

With a Ph.D. in Organic Chemistry and a Master’s in Drug Regulatory Affairs, Sanjiv brings over 18 years of global experience in Regulatory Affairs. He has led strategic submissions across up to 140 countries, developed harmonized regulatory processes, and driven digital transformation initiatives in GRA-RIMS. His expertise spans regulatory intelligence, compliance, dossier development, and health authority interactions.

Currently at CSL Vifor, Sanjiv manages global regulatory activities for key products. His career includes pivotal roles at Roche and Vifor Pharma, where he successfully resolved critical health authority queries, and implemented innovative compliance tools that significantly reduced administrative workload.

In his talk, Sanjiv will share insights on global regulatory key activities - covering NDAs, variations, obligations, and commitments – along with emerging trends. He will also offer practical advice on entering the pharmaceutical industry and building expertise in Regulatory Affairs.

Don’t miss this opportunity to learn from a global Regulatory Affairs expert!