About PRONAV Clinical
Global Expertise, Boutique Service
PRONAV Clinical is a global leader in clinical trial supply chain operations and regulatory consultancy services, with bases in Sligo, Ireland, and Frederick, Maryland, USA.
This strategic positioning allows us to seamlessly access European and US markets, ensuring accessibility, compliance, and timely delivery for clinical trials worldwide.
We’re more than a service provider. PRONAV Clinical is a boutique partner that integrates into your team, providing unrivaled access to our experts and fostering a truly collaborative relationship.
Through regular meetings and transparent communication, we work side by side with you in real-time to navigate the complexities of clinical supply chains and ensure your success.
Who We Are
Mission
To accelerate the delivery of new therapeutics to clinical trials through precision, expertise, and collaborative solutions.
Vision
To be the leading clinical supply chain services provider for early-stage pharma and biotech innovators worldwide.
Meet the PRONAV Clinical Team
Our team combines over 100 years of experience in pharmaceutical operations, quality assurance, and regulatory compliance.
Founder & CEO
Jim Kernan
With extensive experience in authorized and investigational medicines manufacturing, Jim brings a unique combination of C-suite leadership and hands-on expertise in life science manufacturing operations, quality management and regulatory requirements.
Founder and Technical Director
Laurent Borla
Laurent specializes in system qualification, validation, and quality assurance, ensuring flawless execution at every stage.
Head of Global Operations
Orla Kernan
With a degree in Molecular Biology and Genetics, Orla has deep expertise in clinical supply chain services, regulatory compliance, and operational management.
Quality Manager and Qualified Person (EU)
Dr. Anne Kelly
Dr. Kelly is a recognized expert in Quality Management Systems and batch release for a wide range of dosage forms, ensuring compliance with GMP and Regulatory requirements.
Qualified Person (EU)
Feargal Garvin
Feargal’s expertise spans all dosage forms, with specialized experience in biotech batch review and certification.
Why PRONAV Clinical?
At PRONAV Clinical, things work differently. We specialize in reducing and removing the pain points faced by emerging organizations like yours. Working with PRONAV Clinical means gaining a partner who is attentive, engaged, and invested in your success.
No matter your production scale—whether your batch size is 100, 1,000, or 10,000 finished packs—you’ll receive the dedicated attention you deserve. Whether you require single-language or multi-language labelling options, PRONAV Clinical delivers tailored solutions.
At PRONAV, every client, every project, and every patient pack matters.
Our Core Values
Speed:
Our agile and layer-free approach ensures you have immediate access to our project management team and your needs are prioritized.
Precision:
We deliver unmatched precision by combining analytical attention to detail with a comprehensive understanding of your drug product, including its manufacturing and testing pathways, artwork and packaging needs, trial timelines, batch release schedules, and temperature-controlled storage and logistics requirements.
Solutions-Driven:
Fully bespoke roadmaps and a tailored document management system ensure complete visibility and transparency across the entire supply chain. With PRONAV, nothing is hidden—every task and corresponding data file is accessible in near real time, giving you a clear view of current progress and upcoming milestones. Our commitment to transparency means you always know exactly what’s happening and what’s next, empowering you to stay informed and in control at every stage.
Let’s Build Your Success Together
Whether you’re at the preclinical stage or preparing for Phase I trials, PRONAV Clinical is here to accelerate your clinical supply chain journey.