Establish the best possible foundation for your product’s market entry
Long before any therapy goes to market, biopharma companies make decisions that will influence long-term commercial success. That’s why it’s critical to find a trusted strategic partner from the onset that offers services spanning key areas along a product’s life cycle.
Cencora combines scientific expertise and global product development experience to help manufacturers build a solid foundation for a product’s success. We help manufacturers of all sizes around the world to overcome challenges associated with toxicological risk assessment, product and clinical development, clinical trials, and more.
Cencora combines scientific expertise and global product development experience to help manufacturers build a solid foundation for a product’s success. We help manufacturers of all sizes around the world to overcome challenges associated with toxicological risk assessment, product and clinical development, clinical trials, and more.
Why partner with Cencora?
Cencora offers holistic, multi-disciplinary advisory services throughout the early phases of drug development and beyond. Our clients benefit from consulting services across all areas, including early strategic planning for the full commercialization process. This approach avoids a siloed methodology, which can adversely affect a product's cost, timeline, and success.
It is more critical than ever to have the right experts by your side as clinical regulations continue to evolve around the world. We support our clients in Scientific Advice procedures at a national or central level, and in numerous health authority interactions throughout a product’s life cycle.
It is more critical than ever to have the right experts by your side as clinical regulations continue to evolve around the world. We support our clients in Scientific Advice procedures at a national or central level, and in numerous health authority interactions throughout a product’s life cycle.
Our solutions that support drug research and clinical development
Non-clinical services
Increase your product’s likelihood of regulatory acceptance with a comprehensive assessment of potential toxicological risks, demonstrating due diligence with robust data and clear documentation.
Product development strategy
Build a plan with our guidance that establishes the objectives of your clinical program. Align the plan with your requirements and non-clinical data while increasing your ability to meet regional regulatory requirements.
Clinical development support
Navigate successfully through the various phases of clinical development to ensure you create a robust, innovative strategy to maximize asset value and the probability of product success.
Clinical trial support
Overcome clinical trial challenges and enable supply chain transparency at every phase with our suite of trial design, logistics, regulatory, sourcing, and packaging solutions.
Clinical research network
Gain trusted access to qualified patient populations within community-based practices and a time-sensitive approach to eliminate many of the delays typical with study startup.
Clinical biostatistics
Access the level of expertise needed to manage complex trial designs and protocols. Our team interprets datasets and addresses regulatory expectations, particularly in challenging fields.
Our organizations that support drug research and clinical development
As we transition to one Cencora and bring all of our companies and services together under our new name, you can expect a seamless experience no matter which part of our organization you work with. Explore how we serve communities worldwide, backed by global resources and local expertise and support.
