Pharmaceutical Development Group (PDG), Inc.
- North America
- United States
- Human Medicines, Biopharmaceuticals, …
- Service category
- Regulatory services - CMC writing - medical writing, Consulting - strategy and development
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We assist FDA regulated firms in the navigation of the U.S. submission and approval procedures across a variety of dosage forms and therapeutic areas. Our expertise spans prescription and non-prescription (OTC) drugs, biologics and medical devices. we are supported by our full time professional staff and consultants including pharmacologists, epidemiologists, toxicologists, clinicians, analytical scientists, regulatory strategists, business development administrators, labeling experts and others. With extensive combined experience in securing FDA approvals, we are well versed in strategic product planning and regulatory consulting.
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