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Blog Post by Halloran Consulting Group

Halloran Consulting GroupSep 7, 2023 4:39:00 PM5 min read

So, You Have Veeva! Four Tips to Maximize Your Value

The use of Veeva systems, a suite of clinical trial solutions, continues to grow. Veeva’s ...
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Halloran Consulting GroupAug 15, 2023 10:27:00 AM7 min read

How Strong Project Management Propels Clinical Development Success

The Cost and Challenges of Drug Development
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Halloran Consulting GroupAug 3, 2023 4:41:00 PM6 min read

Halloran’s View on FDA’s Draft Guidance on Psychedelic Drugs

The U.S. Food and Drug Administration (FDA) recently issued a draft guidance for industry ...
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Halloran Consulting GroupJul 11, 2023 4:21:00 PM2 min read

Halloran Celebrates 25th Anniversary Milestone

[Boston, Massachusetts, July 10, 2023] – Halloran Consulting Group (Halloran) proudly ...
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Halloran Consulting GroupMay 24, 2023 4:40:00 PM8 min read

Psychedelics as Therapeutics – What Developers Need to Know

Psychedelics as therapeutics are generating great interest from investors and drug ...
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Halloran Consulting GroupMay 7, 2023 5:46:00 PM5 min read

EU MDR Compliance – Why Is Our Industry Still Struggling?

The European (EU) Medical Device Regulation (MDR), adopted in 2017, was a sizeable update ...
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Halloran Consulting GroupMay 1, 2023 5:31:00 PM12 min read

Reimagining Clinical Studies to Support Accelerated Approvals

There is, and always has been, a need for speed in drug development. While, in many ways, ...
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Halloran Consulting GroupApr 18, 2023 11:33:00 AM< 1 min read

A Successful Pre-IND Enabling Next Stage of Development

Regulatory-Case-Study-Pre-IND-1 Download
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Halloran Consulting GroupMar 8, 2023 3:02:00 PM5 min read

Aligning Your Clinical Operating Model – a Case Study by CSL Behring

CONTENT IN COLLABORATION WITH CSL BEHRING Valerie Reynaert, Head of Global Clinical ...
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Halloran Consulting GroupFeb 9, 2023 4:35:00 PM6 min read

Future Proofing Your Clinical Data Infrastructure

Content in Collaboration with eClinical Solutions Written by: Raj Indupuri, CEO, ...
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