As payers focus on long-term outcomes and real-world performance, value matters more than ever. RTI Health Solutions experts discuss how clear evidence storytelling drives access decisions.

As payers focus on long-term outcomes and real-world performance, value matters more than ever. RTI Health Solutions experts discuss how clear evidence storytelling drives access decisions.

Biopharma and medtech explained. Every week, journalists from Fierce Biotech, Fierce Medtech, and Fierce Pharma recount the latest industry trends and why they matter. We'll analyze the week's biggest business news, from mergers and marketing to drug R&D and device development. Available every Friday morning. 

Biopharma and medtech explained. Every week, journalists from Fierce Biotech, Fierce Medtech, and Fierce Pharma recount the latest industry trends and why they matter. We'll analyze the week's biggest business news, from mergers and marketing to drug R&amp;D and device development. Available every Friday morning.&nbsp;

The Top Line

Biopharma and medtech explained. Every week, journalists from Fierce Biotech, Fierce Medtech and Fierce Pharma recount the latest industry trends and why they matter. We’ll analyze the week’s biggest business news—from mergers and marketing to drug R&D and device development. Available every Friday morning.

 

Biopharma and medtech explained. Every week, journalists from Fierce Biotech, Fierce Medtech and Fierce Pharma recount the latest industry trends and why they matter. We&rsquo;ll analyze the week&rsquo;s biggest business news&mdash;from mergers and marketing to drug R&amp;D and device development. Available every Friday morning.
&nbsp;

From approval to value: Why evidence storytelling now matters (Sponsored)

This week on "The Top Line," Fierce Healthcare and Life Sciences' editor-in-chief steps behind the microphone for a solo episode highlighting several of the biggest stories in biopharma.

The episode covers GSK’s first lung cancer approval following its acquisition of Nuvalent, Axiom Biosciences’ unusual plan to list first in Hong Kong before pursuing a Nasdaq co-listing amid a resurgent biotech IPO market, and the U.S. House’s passage of legislation directing the FDA to update its animal testing rules.

The episode also includes an update from the Fierce newsroom, including the arrival of a new Fierce Biotech staff writer, and a reflection on why human judgment, curiosity and original reporting matter more than ever.

To learn more about the topics in this episode: 
GSK secures first lung cancer approval as FDA clears Jideytro in quick payoff from Nuvalent deal
‘There is always a first’: Why US biotech Axiom will begin its IPO journey in Hong Kong
House passes bill directing FDA to update animal testing rules

This week on "The Top Line," Fierce Healthcare and Life Sciences' editor-in-chief steps behind the microphone for a solo episode highlighting several of the biggest stories in biopharma.
The episode covers GSK&rsquo;s first lung cancer approval following its acquisition of Nuvalent, Axiom Biosciences&rsquo; unusual plan to list first in Hong Kong before pursuing a Nasdaq co-listing amid a resurgent biotech IPO market, and the U.S. House&rsquo;s passage of legislation directing the FDA to update its animal testing rules.
The episode also includes an update from the Fierce newsroom, including the arrival of a new Fierce Biotech staff writer, and a reflection on why human judgment, curiosity and original reporting matter more than ever.
To learn more about the topics in this episode:&nbsp;
<ul>
<li><a href="https://www.fiercepharma.com/pharma/gsk-secures-first-ever-lung-cancer-fda-approval-jideytro-nuvalent-deal">GSK secures first lung cancer approval as FDA clears Jideytro in quick payoff from Nuvalent deal</a></li>
<li><a href="https://www.fiercebiotech.com/biotech/axiom-plans-head-nasdaq-hong-kong">&lsquo;There is always a first&rsquo;: Why US biotech Axiom will begin its IPO journey in Hong Kong</a></li>
<li><a href="https://www.fiercebiotech.com/cro/us-house-passes-bill-direct-fda-update-clinical-trial-regulations-and-allow-non-animal-testing">House passes bill directing FDA to update animal testing rules</a></li>
</ul>

GSK’s first lung cancer approval, a new IPO path and more

Clinical trial success depends on more than scientific rigor and operational execution. It also depends on the financial systems that support every stage of a study. In this episode of The Top Line, Zahiah “Zee Zee” Gueddar, senior director of commercial strategy for the Clinical Trial Financial Suite at IQVIA Technologies, discusses why modernizing clinical trial finance has become a strategic priority for sponsors.

As trials become more complex, fragmented systems and manual workflows are creating bottlenecks that limit visibility, delay payments and introduce unnecessary risk. Gueddar explains how these challenges affect site relationships, operational efficiency and study performance, and why organizations can no longer afford to treat finance as a disconnected administrative process.

The conversation also highlights key indicators of readiness for transformation, from cross-functional alignment to executive sponsorship, and outlines the common pain points study teams face today. Ultimately, success depends on moving toward a connected, transparent and predictable financial model that reduces friction, improves collaboration and supports faster, more reliable clinical trials.

Clinical trial success depends on more than scientific rigor and operational execution. It also depends on the financial systems that support every stage of a study. In this episode of The Top Line, Zahiah &ldquo;Zee Zee&rdquo; Gueddar, senior director of commercial strategy for the Clinical Trial Financial Suite at IQVIA Technologies, discusses why modernizing clinical trial finance has become a strategic priority for sponsors.
As trials become more complex, fragmented systems and manual workflows are creating bottlenecks that limit visibility, delay payments and introduce unnecessary risk. Gueddar explains how these challenges affect site relationships, operational efficiency and study performance, and why organizations can no longer afford to treat finance as a disconnected administrative process.
The conversation also highlights key indicators of readiness for transformation, from cross-functional alignment to executive sponsorship, and outlines the common pain points study teams face today. Ultimately, success depends on moving toward a connected, transparent and predictable financial model that reduces friction, improves collaboration and supports faster, more reliable clinical trials.

Why modern clinical trials need a finance-first strategy (Sponsored)

Boston. San Francisco. Beijing? The global biotech industry has long been concentrated in a handful of cities. But which emerging hubs could become dominant forces in biotech in the decades ahead?

In this week’s episode of “The Top Line,” Fierce Biotech’s Darren Incorvaia and Will Maddox discuss a new Fierce special report identifying five cities with the potential to become major forces in the global biotech industry. Did your favorite city make the cut? Listen to find out. 

To learn more about the topics in this episode: 


Top emerging biotech hubs in 2026 


As US lawmakers increase scrutiny of Chinese trials, industry fears ‘huge distraction and expense’ 


British biotech VC funding shows ‘signs of recovery,’ but IPO rebound yet to materialize 


Could Basel be the next Boston? How the Swiss biotech hub is quietly raising its game 

This week's episode is sponsored by IQVIA Biotech.

 
Built for biotech innovators, IQVIA Biotech is a full-service CRO, designed for agility, fast decisions, and the urgency needed for emerging biopharma. With dedicated teams and deep therapeutic expertise, we help move programs forward with focus and confidence. Visit IQVIABiotech.com

Boston. San Francisco. Beijing? The global biotech industry has long been concentrated in a handful of cities. But which emerging hubs could become dominant forces in biotech in the decades ahead?
In this week&rsquo;s episode of &ldquo;The Top Line,&rdquo; Fierce Biotech&rsquo;s Darren Incorvaia and Will Maddox discuss a new Fierce special report identifying five cities with the potential to become major forces in the global biotech industry. Did your favorite city make the cut? Listen to find out.&nbsp;
To learn more about the topics in this episode:&nbsp;
<ul>
<li>
<a href="https://www.fiercebiotech.com/special-reports/top-emerging-biotech-hubs-2026">Top emerging biotech hubs in 2026</a>&nbsp;
</li>
</ul>
<ul>
<li>
<a href="https://www.fiercebiotech.com/biotech/us-lawmakers-increase-scrutiny-chinese-trials-industry-fears-huge-distraction-and-expense">As US lawmakers increase scrutiny of Chinese trials, industry fears &lsquo;huge distraction and expense&rsquo;</a>&nbsp;
</li>
</ul>
<ul>
<li>
<a href="https://www.fiercebiotech.com/biotech/british-biotech-vc-funding-shows-signs-recovery-ipo-rebound-yet-materialize">British biotech VC funding shows &lsquo;signs of recovery,&rsquo; but IPO rebound yet to materialize</a>&nbsp;
</li>
</ul>
<ul>
<li>
<a href="https://www.fiercebiotech.com/biotech/could-basel-be-next-boston-swiss-biotech-hub-raising-its-game">Could Basel be the next Boston? How the Swiss biotech hub is quietly raising its game</a>&nbsp;
</li>
</ul>
This week's episode is sponsored by <a href="https://www.iqviabiotech.com/">IQVIA Biotech.</a>
&nbsp; Built for biotech innovators, IQVIA Biotech is a full-service CRO, designed for agility, fast decisions, and the urgency needed for emerging biopharma. With dedicated teams and deep therapeutic expertise, we help move programs forward with focus and confidence. Visit <a href="https://url.us.m.mimecastprotect.com/s/1v3CCQWBXRslR28JsxfOUGfiN5?domain=iqviabiotech.com/">IQVIABiotech.com</a>

From approval to value: Why evidence storytelling now matters (Sponsored)

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