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Insights From Halloran

Sheila GwizdakNov 25, 2024 12:00:00 AM2 min read

Disrupting the Clinical Trial Ecosystem

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Sheila GwizdakNov 20, 2024 5:57:18 PM3 min read

Moving Through Clinical Development and Operations Obstacles on the Path to Commercialization

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Halloran Consulting GroupOct 15, 2024 11:12:42 AM8 min read

Three Key Impacts in 2025: Fundraising, ICH E6(R3), and Policy

A Q&A featuring Tania Zieja, President of Halloran Consulting Group.
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Lyn AgostinelliAug 21, 2024 12:45:00 PM2 min read

483 Issues to Sites – Indicators of Sponsor Oversight Effectiveness

A U.S. Food and Drug Administration (FDA) Form 483 is issued to a company’s management at ...
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Halloran Consulting GroupAug 2, 2024 11:30:00 AM7 min read

How, Why, and When to Apply for an Orphan Drug Application

This article is written by Hema Balasubramanian and Mamta Puri-Lechner. In the rapidly ...
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Halloran Consulting GroupJul 10, 2024 3:57:00 PM5 min read

Catching Up with Consulting — DIA 2024 Insights

This article is based on opinions and perceptions from the DIA 2024 Global Annual ...
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Gail WinslowJul 3, 2024 4:00:00 PM4 min read

Generative AI-Driven Clinical Trials: Are We There Yet?

This article is based on the session titled, “Generative AI-Driven Clinical Trials: Myth ...
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Gail WinslowJul 1, 2024 12:35:00 PM4 min read

Maximizing The Next 40 Years of The Orphan Drug Act 

This article is based on the session titled, “Sustainability of Rare Disease Drug ...
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Rebecca Shorin, PMPJun 12, 2024 8:57:00 AM4 min read

Future of Clinical Trials: Forging New Pathways with Artificial Intelligence  

Biocom California’s first annual Converge Summit, recently held in South San Francisco, ...
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Katie W McCarthyMay 15, 2024 12:15:00 PM4 min read

Investors Follow Teams: Leadership Considerations to Enable Success 

Developing a life science asset from early discovery through clinical development to ...
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