Turning a herbal formulation into an approved and market-ready drug requires going through scientifically validated preclinical and clinical trial stages. At Padideh Giah, we offer comprehensive support to startups, researchers, and pharmaceutical companies seeking to develop safe and effective herbal products.
Turning a herbal formulation into an approved and market-ready drug requires going through scientifically validated preclinical and clinical trial stages. At Padideh Giah, we offer comprehensive support to startups, researchers, and pharmaceutical companies seeking to develop safe and effective herbal products.
Design and execution of acute and subacute toxicity studies
Pharmacokinetic analysis (absorption, metabolism, and elimination) of herbal actives
In vitro (laboratory) and in vivo (animal) biological studies
Standardization of herbal extracts and identification of active compounds
Protocol design consultation for clinical trials (Phases I–IV)
Collaboration with certified clinical research centers for trial execution
Clinical data analysis and documentation for regulatory submissions
Full project management for herbal drug R&D
Access to a strong network of scientific and clinical partners
Lower risk of regulatory rejection through international-standard design
End-to-end support for herbal drug dossiers and FDA-equivalent approvals
Whether you're launching a herbal startup or advancing a new botanical product, we are here to guide you through every critical step—from lab to market.
