Key Capabilities for Prescription Drug Development

Innovative Prescription Drug Formulations 

• Development of prescription-strength creams, gels, foams, sprays, and patches
• Controlled-release and enhanced permeation technologies for optimized drug delivery
• Formulation of high-potency prescription products with specialized handling
• Customization for targeted therapy applications

Regulatory Compliance and NDA/505(b)(2) Submissions 

• Comprehensive regulatory support for New Drug Applications (NDA)
• 505(b)(2) pathways for reformulated or improved prescription drugs
• GMP-compliant manufacturing ensuring patient safety and efficacy
• CMC documentation preparation for FDA and global regulatory filings

GMP-Standard Manufacturing and Quality Control 

• Full-scale production of prescription topical and transdermal drugs
• GMP-certified facilities with stringent quality assurance
• End-to-end stability and bioavailability testing for long-term safety
• Packaging and serialization for regulatory compliance and market readiness

Why Choose MedPharm for Prescription Drug Development?

• Industry-Leading Expertise in Prescription Topical and Transdermal Formulations
• Regulatory-Compliant NDA and 505(b)(2) Drug Development
• GMP-Certified Facilities Supporting Clinical and Commercial Manufacturing
• Comprehensive Analytical and Stability Testing for Market-Ready Products
• Customized Drug Delivery Solutions for Enhanced Patient Compliance

Advance Prescription Drug Innovation with MedPharm’s Expertise

With scientifically optimized formulations, regulatory-driven quality assurance, and state-of-the-art manufacturing, MedPharm ensures that your prescription drug products achieve optimal therapeutic performance and commercial success.