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Featured Case Studies

Insight-driven and inventively bold, we excel in building strategies and developing highly customized programs. Our experience—from custom-designed clinical research studies to FDA registration and approval to commercialization—allows us to establish the best path to optimal outcomes.


Combination Product Expertise and Target Market Knowledge Create Commercial Success

By identifying the proper product category, we worked with an international company to correctly reposition its drug-device combination product for FDA approval and drive market penetration.

Read Regulatory & Strategic Development Case Study

 

Real World Evidence Saves Project

When a biotech company could not afford the time and expense to conduct intended studies, we stepped in and quickly and creatively turned things around with the FDA.

Read FDA Product Development & Regulatory Consultant Case Study

 

Rapid Nonclinical Planning and Coordination Keep Post-Marketing Requirements on Track

After a biotech company received paper NDA approval for their drug, Camargo contributed to successful commercialization, planning and executing Phase 4 post-marketing requirements with a short timeline.

Read Post-Marketing Nonclinical Case Study

 

Strategic Submission Preparation Redefines Product Value

With strategic submission support, a biotech company gained approval for an improved delivery technology of an already-approved drug, setting the potential to become a new “gold standard” treatment in oncology.

Read Strategic Submission Case Study


Camargo Pharmaceutical Services provides comprehensive drug development solutions, specializing in customized programs including the 505(b)(2) pathway.


Contact
Headquarters
9825 Kenwood Road
Suite 203
Cincinnati OH, 45242
Durham Office
800 Taylor Street
Suite 101
Durham NC, 27701
Montreal Office
507 Place d'Armes
Suite 1101
Montreal, QC H2Y 2W8, Canada
Phone 513.561.3329
Toll Free 888.451.5708
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