Pharmaceutical Development Group

Pharmaceutical Development Group (PDG) assists firms in the navigation of the U.S. FDA 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 and supplements. PDG possesses the resources and experience to address large scale development projects, long-term regulatory strategies and complex non-clinical and clinical issues. We can quickly and efficiently address unexpected emergencies and often faster than large companies can perform in-house. PDG maintains a posture of readiness to react and respond to your regulatory needs 24 hours a day, 7 days a week. We recognize that you may receive an FDA Form 483 or Warning Letter, may be faced with the possibility of a recall, or have encountered some other sudden and urgent situation. Regardless of the emergency, as your FDA regulatory consultant, PDG is always ready to respond ...