Pharmaceutical Consulting
Regulatory Consulting
FDA Approval Services
FDA Inspection

Pharmaceutical Development Group Inc. (PDG) was founded in 1999 by Dr. Cheryl Blume and has quickly become a leading consulting firm serving both the pharmaceutical industry and the legal community. Headquartered in Tampa, Florida, PDG is involved in a wide variety of regulatory and pharmaceutical development assignments designed for both the U.S. and international registration and compliance purposes.

PDG assists pharmaceutical firms in the navigation of the U.S. submission and approval procedures for all products regulated by the FDA. PDG is also a recognized leader in providing regulatory consulting to organizations of all sizes, both foreign and domestic. Additionally, PDG serves as an expert in drug related litigation including regulatory support services, the compilation of expert reports, deposition testimony and trial testimony.

PDG is supported by a comprehensive consortium of experienced pharmacologists, toxicologists, clinicians, analytical scientists, regulatory strategists and business development administrators. With over 200 years of combined experience in securing drug product approvals, both nationally and internationally, PDG is well versed in strategic product planning and regulatory consulting. To learn more about our services, please browse through our website and feel free to contact us at any time.