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OUR SERVICES

We take a personalized and integrated approach to help our clients position their pipelines and companies for success offering a full range of development and commercialization services.

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PHASES
DISCOVERY
Uncover breakthrough
innovations during the drug
discovery phase.
CLINICAL DEVELOPMENT
Advance through clinical
development and health
authority review with confidence.
ALL STAGES
Benefit from our expertise
across all phases
of drug development.
PRECLINICAL
Navigate the critical
preclinical testing phase
with expert guidance.
COMMERCIALIZATION
Successfully bring your
product to market with
our commercialization support.
ALL SERVICES
Access comprehensive
services for every stage
of product development.

ABOUT US

We are Halloran, a life science consulting firm, partnering to enrich your product development and business growth. We propel your organization further; positively impacting the health and wellbeing of patients around the world.

LEARN MORE ABOUT US
EXPERTISE WITH PERSONALITY
OUR FOUNDER
Discover the visionary
leader driving Halloran's
success and innovation.
STRATEGIC PARTNERS
Meet our trusted
strategic partners who
enhance our capabilities.
WHY HALLORAN?
Explore the unique reasons
why clients choose
Halloran for their needs.
OUR TEAM
Get to know the dedicated
professionals who make
up the Halloran team.
CAREERS
Join our dynamic team
and advance your
career with Halloran.
CASE STUDIES
Learn Halloran’s unique
strategy and approach to address
the pressing needs of our clients.
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Insights From Halloran

Carolina Ahrendt, MBA, PMPMay 22, 2025 9:45:53 AM1 min read

Mastering Program Management and Leadership: Five Pillars to Drug Development Excellence Webinar

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Shawn Roach, PhD, RACMay 16, 2025 11:18:11 AM2 min read

Halloran’s Regulatory Lens – What We’re Watching in 2025

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Platform Promise vs Regulatory Reality: Navigating Product-Specific Expectations in Cell and Gene Therapy

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Josh WootenMay 8, 2025 7:57:17 AM1 min read

Start it off Right: The Importance of Building an IND from High-Quality Nonclinical Reports

Nonclinical reports are one of the most critical pieces for building an IND, but are ...
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Meghan Patterson, MPHMay 2, 2025 11:23:42 AM3 min read

Balancing Simplicity and Complexity in Clinical Trial Design

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Steve Kornher, PhDApr 28, 2025 3:12:28 PM8 min read

Risk Mitigation Planning for Pharmaceutical Tariffs

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Meghan Patterson, MPHApr 22, 2025 12:32:06 PM4 min read

ICH E6(R3) and a Risk-Based Approach as a Competitive Advantage 

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Elizabeth BodiApr 14, 2025 5:52:43 PM1 min read

Key Update on Guideline for Good Clinical Practice E6(R3)

January 6, 2025: ICH assembly agreed that ICH GCP E6 R3 Principles and Annex 1 could be ...
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Mike Fusakio PhDApr 14, 2025 4:38:00 PM2 min read

Impact on Product Development: FDA Phasing Out Animal Testing Requirement

Contributing Author: Hema Balasubramanian The FDA announcement on its plan to phase out ...
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Carolina Ahrendt, MBA, PMPApr 10, 2025 12:40:26 PM6 min read

Ticking Timeline: Tips for Effective Product Development Timelines

Once a biotech or pharmaceutical company defines their product development objectives ...
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