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MedPharm offers a suite of expert services designed to support clients at every strategic and operational phase of pharmaceutical development to give you enhanced clarity, confidence, and compliance.
Scalable, GMP-Compliant Production for Market Success
MedPharm offers fully scalable, GMP-certified manufacturing solutions to ensure consistent, high-quality topical and transdermal formulations production. We support pharmaceutical companies from the final stages of drug development to full-scale commercial supply by utilizing advanced production technologies, strict quality control measures, and regulatory-compliant processes.
Since 1999, MedPharm has established a strong reputation for delivering exceptional solutions to our clients. We help them navigate the complexities of topical and transdermal product development, ensuring they take the most effective formulation to the clinic.
Since 1999, MedPharm has established a strong reputation for delivering exceptional solutions to our clients. We help them navigate the complexities of topical and transdermal product development, ensuring they take the most effective formulation to the clinic.
Innovative, Science-Driven Formulation Strategies for Topical & Transmucosal Drug Products Comprehensive Formulation Development Services
At MedPharm, our Analytical Services are not just a checkpoint—they are a strategic cornerstone of successful pharmaceutical development. We specialize in topical and transdermal drug products, providing analytical and bioanalytical testing to support every phase of the product lifecycle, from early-stage formulation to clinical development and commercial release.
– Pre-formulation studies and API characterization
– Target product profile (TPP) development
– In silico and in vitro assessments for drug viability
– Formulation screening and optimization for lead candidates
– IND-enabling studies and regulatory support
– Scale-up manufacturing and technology transfer
– GMP production for Phase II and III clinical trials
– Analytical method development and validation
– Stability studies and ICH-compliant testing
– Process validation and regulatory submission support
At MedPharm, we recognize that clinical supply goes beyond logistics—it’s a vital component in proving the viability, safety, and efficacy of your drug product. Our Clinical Supply Services provide comprehensive support for topical and transdermal clinical programs, ensuring that your investigational therapies are manufactured, tested, and delivered with precision and compliance.
– Large-scale GMP manufacturing for market supply
– Quality control testing and batch release
– Regulatory compliance with global market requirements
– Lifecycle management and continuous process improvement
– Supply chain and distribution support for commercial products
