Biopharma manufacturers face significant challenges when advancing new therapies from concept to market. Every stage of the process—research, clinical trial design, regulatory navigation, pharmacovigilance, and logistics—carries risks that can delay development or compromise compliance. Cencora’s drug research and clinical development services are designed to reduce those risks by providing integrated expertise, global reach, and technology-driven solutions. By combining scientific insight with operational support, Cencora helps manufacturers streamline processes, protect patients, and build a stronger foundation for long-term commercial success.
Key areas of functionality include:
- Clinical Development Consulting
- Regulatory Support
- Pharmacovigilance Software and Services
- Clinical Data Software and Services
- Trial Master File (TMF) Solutions
- Clinical Trial Operational Design
- Clinical Trial Supply Chain and Logistics
- Clinical Research Network
This approach allows manufacturers to move therapies forward with greater efficiency, compliance, and confidence. If you’d like a breakdown of how these services align with your current development strategy, Cencora offers tailored guidance.
