From Early Development to Commercialization At MedPharm, we provide end-to-end drug development and manufacturing solutions across all development stages, from preclinical research to commercial production. Our scientifically driven approach, regulatory expertise, and GMP-compliant facilities ensure that every formulation is optimized for safety, efficacy, and scalability, allowing for a seamless transition through clinical and commercial phases. With state-of-the-art formulation development, analytical testing, and process optimization capabilities, MedPharm helps pharmaceutical companies accelerate development timelines, navigate regulatory pathways, and bring innovative therapies to market successfully. Seamless Integration of Development and Manufacturing
– 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
– 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