We’re a boutique, full-service CRO operating globally with lean teams and high-value assets. We take a hands-on approach, delivering flexible engagement models, ensuring complete pricing transparency, and taking ownership of projects – without adding unnecessary overhead.
With hundreds of trials delivered, we focus on therapeutic areas where innovation is most needed, including oncology, cardiology, and rare diseases, with a particular emphasis on nuclear medicine. We offer an Integrated Digital Clinical Trial Solution, delivering flexible engagement models tailored to your needs with maximum transparency, scalability, and cost efficiency.
Our promise? Faster, smarter, leaner clinical trials – without compromise. Axcellant in every aspect.
years of experience
clients
trials delivered
sites supported
patients enrolled
Our senior team remains closely involved in the whole process – from strategy and protocol design through execution and readout, ensuring patient impact stays at the core while minimizing amendments and accelerating study start-up.
We combine deep scientific expertise with purpose-built digital tools and a modular platform that adapts to each study. This sharpens feasibility, site and patient selection, and monitoring, while providing real-time visibility into enrollment, safety, and operational KPIs—no chasing updates. The result is right-first-time execution and submission-ready packages for FDA and EMA—smarter, safer, more adaptable trials that deliver investor-grade evidence.
Leveraging extensive knowledge in nuclear medicine and diverse imaging modalities, including Imaging Core Lab support, we deliver high-quality data and expert guidance to enhance the success of your study.
Leveraging extensive knowledge in nuclear medicine and diverse imaging modalities, including Imaging Core Lab support, we deliver high-quality data and expert guidance to enhance the success of your study.
Read MoreOur team secures medical device development with pre- and post-market planning, ensuring compliance with FDA CFR, ISO, and MDR standards.
Our team secures medical device development with pre- and post-market planning, ensuring compliance with FDA CFR, ISO, and MDR standards.
Read MoreWe support clients from early-phase strategy to regulatory approval every step of the way. Design and manage clinical trials that generate high-quality, regulatory-compliant data across all development phases.
We support clients from early-phase strategy to regulatory approval every step of the way. Design and manage clinical trials that generate high-quality, regulatory-compliant data across all development phases.
Read MoreAxcellant’s team guarantees streamlined, end-to-end clinical trial execution. Our experienced team ensures the delivery of timely, compliant, and cost-effective studies tailored to meet your goals.
Axcellant’s team guarantees streamlined, end-to-end clinical trial execution. Our experienced team ensures the delivery of timely, compliant, and cost-effective studies tailored to meet your goals.
Read MoreWith expertise in statistical modelling, programming, and data collection methodology, we deliver accurate and reliable insights to support your research and decision-making.
With expertise in statistical modelling, programming, and data collection methodology, we deliver accurate and reliable insights to support your research and decision-making.
Read MoreOur regulatory team specializes in crafting effective regulatory strategies and ensuring compliance throughout the project lifecycle. From initial planning to completion, we provide expert guidance to navigate complex regulatory frameworks with precision and efficiency.
Our regulatory team specializes in crafting effective regulatory strategies and ensuring compliance throughout the project lifecycle. From initial planning to completion, we provide expert guidance to navigate complex regulatory frameworks with precision and efficiency.
Read MoreWe ensure timely detection, assessment, and reporting of adverse events in full compliance with FDA, EMA, and global pharmacovigilance regulations. Our services prioritize patient protection and uphold the highest product safety standards throughout the lifecycle.
We ensure timely detection, assessment, and reporting of adverse events in full compliance with FDA, EMA, and global pharmacovigilance regulations. Our services prioritize patient protection and uphold the highest product safety standards throughout the lifecycle.
Read MoreOur robust systems, streamlined processes, and comprehensive training programs have demonstrated excellence through numerous successful audits and inspections, ensuring the highest compliance and quality standards.
Our robust systems, streamlined processes, and comprehensive training programs have demonstrated excellence through numerous successful audits and inspections, ensuring the highest compliance and quality standards.
Read MoreOur resourcing division collaborates closely with you to identify and fulfil your specific needs, providing flexible and tailored solutions to support your operations.
Our resourcing division collaborates closely with you to identify and fulfil your specific needs, providing flexible and tailored solutions to support your operations.
Read MoreOver the years we have supported organisations across many therapeutic areas, from various medicinal products phase I or medical devices pilot programmes through to very niche esoteric clinical packages of activity.
Our passion for science, an unwavering commitment to improve the lives of patients and an unflagging energy to deliver on commitments has enabled us to gain broad expertise.
We’re pleased to announce a strategic partnership between Axcellant and Prometheus MedTech.AI — a medtech startup developing AI-powered solutions for…
The Axcellant team has returned from the European Association of Nuclear Medicine (EANM) Annual Congress in Barcelona — and it’s…
The robust development of nuclear medicine depends on the availability of radioactive isotopes, some of which are used for diagnostic…
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