The Future of UK Life Sciences Regulation

Navigate Regulatory Complexity with Confidence — Meet tranScrip’s Experts 1:1

Are you preparing for your next regulatory submission, facing feedback from the EMA or MHRA, or planning for early scientific advice? Secure a one-on-one session with tranScrip’s regulatory experts during conference breaks to discuss your toughest challenges. 

Whether you’re:

  • Struggling to define the right regulatory strategy for your development phase,
  • Seeking clarity on evolving EU or UK regulatory frameworks,
  • Wondering how to accelerate approval timelines,
  • Or exploring how to optimise interactions with agencies

The tranScrip team will help you navigate complexity and drive your programme forward with confidence.

Don’t miss this opportunity to gain strategic insights from leaders who have successfully guided products from first-in-human trials to market approval.

Spaces are limited — book your 1:1 meeting in advance to secure your slot.

View tranScrip's webpage here.

Markas Marriott

Markas Marriott

Executive Director, Regulatory Affairs, tranScrip Ltd

Jon Sisson

Jon Sisson

Executive Medical Director, Clinical Development & Regulatory Strategy, tranScrip Ltd