PharmaceuticalDevelopmentGroup –

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.

Pharmaceutical regulatory consulting
Medical device consulting
ind consulting
Pharmaceutical scientist
Drug monograph format
Adaptive design clinical trials
Post marketing safety surveillance
Regulatory affairs services
510(k) submission
Pharmacovigilance consultants

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