Market Access Consulting
Our unique approach emphasizes the importance of envisioning commercial success from the very beginning, ensuring that each step in the trial not only meets scientific standards but also aligns with broader market strategies and future demands.
Strategic Pre-Trial Consulting: Integrating Commercialization Vision from the Outset.
By employing a partnership model, we collaborate closely with our clients to design and execute commercially driven clinical trials.
Commercial Opportunities
We provide comprehensive commercialization opportunities by analyzing market size, identifying gaps, benchmarking against competitor pricing, and assessing potential through EPI programs and government tenders. This holistic approach ensures our clients are strategically positioned for optimal market penetration and growth.
Local Manufacturing
We offer expertise in local manufacturing, providing guidance on potential opportunities, introducing clients to Contract Manufacturing Organizations (CMOs), and facilitating technology transfer support. This comprehensive service ensures seamless integration into the local production landscape and efficient tech adaptation.
Clear Regulatory Pathways
We provide a clear regulatory pathway by identifying countries ripe for local registration based on trial outcomes and pinpointing nations with mature regulatory systems recognized by WHO or EMA. This strategic approach ensures efficient market entry and alignment with top-tier regulatory standards.
GMP Requirements and QP Certifications
We assist clients in navigating the diverse GMP requirements across countries and offer solutions for EU QP declarations, ensuring products meet quality standards and facilitating smoother market entry within the European Union.
Clinical Trial Execution Excellence
We support clients by ensuring their protocols are accepted by EC/RA authorities, identifying locations with relevant disease prevalence, connecting them with experienced sites and principal investigators upholding global standards, and implementing accelerated patient recruitment strategies. This comprehensive service facilitates a faster, efficient, and globally-aligned clinical trial process.
Global Coverage
Celero Executive team have experience in 80 trials across multiple clinical development phases (P1-P4) in more than 29 countries (US, EU, LATAM, APAC and Africa).
Introducing the Celero Way
A pathway to high-quality, cost-controlled, accelerated trials tailored to your needs.
Learn more about The Celero Way or speak to our Market Access expert.
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We are successfully ISO 9001 certified, which further underscores our commitment to meeting internationally recognized quality standards for quality, reliability, and excellence.