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Cardinal Health Specialty Solutions delivers proven regulatory consulting expertise to help you obtain global product approval, assist in securing financing and maintain filings throughout the entire product lifecycle.
Our 200 expert consultants have an average of over 15 years of industry and FDA experience.
Our regulatory experts have worked successfully with global regulatory agencies and every review division of the FDA. We have provided support for more than 100 New Drug Application (NDA), Biologic License Application (BLA) and Abbreviated New Drug Application (ANDA) approvals and has provided drug development services for new drugs in all major therapeutic areas.