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.

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. 

Innovative, Science-Driven Formulation Strategies for Topical & Transmucosal Drug Products Comprehensive Formulation Development Services

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.

IVRT provides regulatory-compliant drug release assessments, evaluating formulation performance by measuring drug diffusion over time. It is an essential tool for optimizing formulations and for bioequivalence studies in both generic and innovator drug development. 

Ensure your analytical methods are scientifically sound and compliant with ICH Q2(R1) guidelines, whether they were developed in-house or transferred from your team.

Innovative, Science-Driven Formulation Strategies for Topical & Transmucosal Drug Products Comprehensive Formulation Development Services

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.

For safety, efficacy, and metabolism assessments, MedPharm utilizes reconstructed human epithelium models. This approach allows for accurate, ethical, and reproducible evaluations of topical and transdermal formulations.

By employing automation and rapid screening techniques, our high-throughput permeation testing accelerates early-stage development, enabling us to quickly identify the most effective formulations.

As a gold-standard technique, IVPT assesses drug penetration through biological membranes, providing critical data for product development and regulatory submissions. Our expertise encompasses studies involving human and animal skin, mucosal tissues, and specialized reconstructed epithelial models. 

MedPharm specializes in testing for ungual and hard tissue formulations, assessing drug penetration into nails, calloused skin, and keratinized structures to support product efficacy and optimization.