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Strategic Drug Development Consulting Services

Reduce drug development time to maximize your returns on research investments

The regulatory consulting team at Cardinal Health Specialty Solutions provides drug development consulting services to help minimize risk during development and reduce the time required to obtain product approval.  Our experts have experience providing regulatory and product development consulting services for the development of new drugs in all major therapeutic areas.
Through our experienced professionals and network of recognized consultants , we have become industry leaders in successfully navigating the maze of requirements for the FDA and other global regulatory agencies. Our focus is to help pharmaceutical, biotechnology and medical device companies receive timely product approvals and increase the financial returns on their research investments.

Drug development areas of expertise

  • Human and animal health
  • Orphan drugs
  • Small molecules and biological products
  • New chemical entities and generic product development
  • Active pharmaceutical ingredients (APIs)
  • Finished products
  • Medical devices

Case Study: Bringing a New Drug to Life

How we guided a pharma company’s breakthrough vision to commercial reality.

William (Trey) C. Putnam, PhD, RAC

Lavonne M. Patton, PhD

Director, Regulatory Affairs and Product Development

Diane Beatty

Diane M. Beatty, PhD

Managing Director, Regulatory Affairs and Product Development

Investigational and Marketing Application Services

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504KB – PDF

Biotechnology Consulting Services

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537KB – PDF