tranScrip Talks cover art

tranScrip Talks

tranScrip Talks

By: tranScrip
Listen for free

About this listen

Welcome to tranScrip Talks, the podcast for biotech and pharma companies seeking strategic, practical, and expert-led guidance across the entire product lifecycle, from TRANslation to preSCRIPtion. Brought to you by the experts at tranScrip, each episode explores the most pressing challenges and breakthrough opportunities across early and clinical development, market access and commercialisation, regulatory and medical affairs, pharmacovigilance and more.

Expect real case experience, actionable insights and forward-thinking strategies, all designed to help you accelerate and optimise the path from molecule to market.

Copyright 2025 All rights reserved.
Biological Sciences Science
Episodes
  • Episode 4 | Where Regulatory Meets Medical: The Key to De-Risking Drug Development
    Jan 21 2026

    Christopher Floyd, Executive Medical Director, is joined by Roz Sutton, Regulatory Expert, to explore how regulatory and medical alignment plays a critical role in de-risking drug development. They discuss why regulatory strategy must be shaped early, how medical rationale strengthens regulatory decision-making, and what it takes to execute with confidence in an evolving landscape.

    Show More Show Less
    25 mins
  • Episode 3 | Racing Against Resistance: The Future of Antimicrobial Innovation
    Oct 29 2025

    Rienk Pypstra, tranScrip’s Chief Medical Officer, joins Marc Lemonnier, Chief Executive Officer of Antabio, to discuss the global threat of antimicrobial resistance. They’ll explore why innovation must outpace bacterial evolution, how economic incentives can sustain antibiotic R&D, and why agility, collaboration, resilience and strategic vision are essential to overcoming resistance and driving the future of AMR.

    Show More Show Less
    23 mins
  • Episode 2 | Getting Ready for Clinic
    Sep 17 2025

    Rob Fox, tranScrip’s Chief Commercial Officer, joins Dr Christopher Floyd, Executive Medical Director, Early Development, to discuss the leap from preclinical to clinical. They’ll explore why it’s critical to weave a compelling translational narrative, design adaptive first-in-human studies, treat regulators as partners, focus on clarity over clutter in data, avoid decision paralysis and build expert teams aligned for success from day one.

    Show More Show Less
    26 mins
No reviews yet