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July 22, 2020

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Tampa, FL

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Pharmaceutical Development Group (PDG) assists FDA regulated firms in the navigation of the U.S. submission, approval and post-marketing procedures across a variety of dosage forms and therapeutic areas. Our expertise spans prescription and nonprescription (OTC) drugs, both NDA and monograph, as well as devices. While PDG possesses the resources and experience to address large scale development projects, long-term regulatory strategies and complex non-clinical and clinical issues, we remain as nimble and responsive as the day of our founding.
otc product development
combination drug product
combination pharmaceutical development
review of drug product labeling
pharmaceutical industry news
literature search services
combination device and drug
generic drug product development