Characterizing the patient experience: The role of patient‑reported outcomes 

By Aurora Berra, Head of Global Patient Affairs  Biological endpoints are essential, but on their own, they cannot tell the

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A bridge to the field: how real-world data informs rare disease care

“We try to identify and understand how to better support patients outside the context of clinical trials.”  As a Field

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Rethinking discovery: how powerful screening tools are redefining the search for new medicines

By Mary Jane Hinrichs, SVP Head of Early Development and Innovation In medicine discovery, identifying the right biological target has

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When science advances, understanding must keep pace

Aurora Berra, Vice President Global Patient Officer We are living in an era of extraordinary scientific progress. We can target

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Why evidence matters: Seema Meloni on making data meaningful  

“In order to help all partners understand the value of a medicine, we provide the wrap-around support of data coming

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From molecule to medicine: the process behind patient-ready treatments

“We need to make sure that it’s scalable, safe, and reproducible—so that every patient gets the same medicine every time.”   As

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When bile acids tell a bigger story: how cholestatic biology is reshaping rare liver disease research 

. Jennifer Schranz, Senior Vice President, Head of Rare Diseases   The human cost of a system out of balance   Over

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Testing the hypothesis: a focused pilot for AI in healthcare

Every scientific breakthrough begins with a question: can this medicine extend life, restore balance, or meaningfully change what is possible

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Always one step ahead: Anne Petit on making medicines happen

Anne Petit does not wait for instructions. She knows that in pharmaceutical development, her team often moves first. “We always

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From data to decisions: how Ipsen turns medical data into action for patients

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