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Pharmaceutical Development Group (PDG) is a subsidiary of Biotech Research Group Corporation.
+1.813.333.2950
[email protected]
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PDG
Pharmaceutical Development Group
Home
Services
Pharmaceutical Consulting Services
Strategic Drug Development
Strategic Drug Development Services
Pharmaceutical Development Programs: Implementation and Oversight
Pre-IND Meetings
Investigational New Drug Application (IND)/Special Protocol Assessment (SPA)
Clinical Trial Design
Pre-NDA Meetings and NDA Submissions: 505(b)(1)/505(b)(2)
505(b)(2) NDAs
Generic Drugs: 505(j) ANDAs and Potential Diversification
Nonprescription Drugs (OTC)
Medical Device Consulting
Exempt Devices / 513(g) Submissions
Device Pre-submission Meetings and Reviews
Facility Inspection Readiness
Combination Device and Drug/Biologic Submissions
510(k) Submissions
PMA Submissions
Post-Launch Activities
Drug Post-Launch Activities
Post-Marketing Surveillance
Drug Labeling
Specialty Services
Specialty Services
Citizen Petitions
Legal Support
Literature Searches
Pharmacokinetic Consulting
Quality Assurance & Compliance
Scientific and Technical Writing
Supplier/Vendor Selection and Qualification
Toxicology Consulting
Regulatory Updates
About PDG
About PDG – An FDA Regulatory Consultant
Your Pharmaceutical Consultant
Careers at PDG
Regulatory Resources
Regulatory Resources
FDA Links
International Health Authority’s Websites
Contact PDG
Home
Services
Pharmaceutical Consulting Services
Strategic Drug Development
Strategic Drug Development Services
Pharmaceutical Development Programs: Implementation and Oversight
Pre-IND Meetings
Investigational New Drug Application (IND)/Special Protocol Assessment (SPA)
Clinical Trial Design
Pre-NDA Meetings and NDA Submissions: 505(b)(1)/505(b)(2)
505(b)(2) NDAs
Generic Drugs: 505(j) ANDAs and Potential Diversification
Nonprescription Drugs (OTC)
Medical Device Consulting
Exempt Devices / 513(g) Submissions
Device Pre-submission Meetings and Reviews
Facility Inspection Readiness
Combination Device and Drug/Biologic Submissions
510(k) Submissions
PMA Submissions
Post-Launch Activities
Drug Post-Launch Activities
Post-Marketing Surveillance
Drug Labeling
Specialty Services
Specialty Services
Citizen Petitions
Legal Support
Literature Searches
Pharmacokinetic Consulting
Quality Assurance & Compliance
Scientific and Technical Writing
Supplier/Vendor Selection and Qualification
Toxicology Consulting
Regulatory Updates
About PDG
About PDG – An FDA Regulatory Consultant
Your Pharmaceutical Consultant
Careers at PDG
Regulatory Resources
Regulatory Resources
FDA Links
International Health Authority’s Websites
Contact PDG
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