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At Genie Pharma, we believe the future of healthcare depends on more than science alone — it requires vision, collaboration, and a commitment to doing what’s right. From molecule to market, we partner with innovators worldwide to develop, manufacture, and deliver high-quality, cost-effective active pharmaceutical ingredients (APIs) and finished formulations.
Our leadership team brings a combined experience of over 100 years in pharmaceutical innovation, USFDA/EDQM-compliant manufacturing, regulatory strategy, and commercial scale-up. Their expertise spans building greenfield manufacturing sites, leading global R&D programs, and securing successful product launches in over 70 countries.
Innovative and client-centric research support including process development, analytical method development, and technology transfer, guided by scientific rigor and regulatory standards.
Reliable and scalable manufacturing solutions for APIs and intermediates, ensuring quality, cost-efficiency, and timely delivery across all phases—from clinical to commercial scale.
NCustom synthesis of known, unknown, and stable-labeled impurities with structural elucidation, characterization, and regulatory documentation to support impurity profiling and ICH compliance.
Polymorph screening and selection to enhance bioavailability, stability, and IP positioning—helping you choose the optimal solid form for development and commercialization.
Comprehensive Chemistry, Manufacturing, and Controls (CMC) services supporting IND, NDA, and ANDA submissions, with meticulous documentation and technical support across all development stages.
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