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.
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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.
In this episode, host Dr Rienk Pypstra, tranScrip’s Chief Medical Officer, joins David Findlay, CEO of Rostra Therapeutics, to lay out the essential blueprint for biotech success.
They’ll explore why it’s vital to:
· Define a laser-focused vision & mission
· Build an early Target Product Profile
· Win investor confidence with a data-driven route to market
· Engage regulators from day one to de-risk development
· Select partners who add real value, not just capacity
tranScrip Talks
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.
