We are actively expanding our content for the following solutions. Please visit again soon to explore the new pages:
- Clinical development consulting
- Regulatory support
- PV software and services
- Clinical data software and services
- Clinical trial operational design
- Clinical trial logistics
- Clinical trial product strategy
- Clinical research network
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
Clinical development consulting
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 development regulatory support
Maintain compliance and facilitate approvals by navigating regulatory requirements, from trial initiation to completion. Align activities with the latest regulatory standards and best practices with our guidance.
Clinical pharmacovigilance software and services
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 data software and services
Advanced data management solutions offer accurate and efficient data collection and analysis throughout clinical trials. Accelerate clinical trial timelines with rapid data analysis.
Trial master file software and services
Achieve TMF health and maintain inspection-readiness with our software and services. We help you simplify and streamline the entire TMF management process.
Clinical trial operational design
Design efficient and effective trial operations, optimizing protocols for success and compliance. Reduce trial execution times and accelerate access to to new therapies.
Clinical trial supply chain and logistics
Overcome clinical trial challenges and enable supply chain transparency at every phase with our suite of trial design, logistics, regulatory, comparator sourcing, and packaging solutions.
Clinical trial product 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 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.
Featured therapeutic expertise
Our organizations that support drug research and clinical development
As one Cencora, we have worked to bring all of our companies and services together to make sure you can expect a seamless customer experience. Explore how we serve communities worldwide, backed by global resources, local expertise, and support.
