Drug-development

Understand the complete lifecycle of drug development—from discovery to post-market surveillance—aligned with global regulatory requirements.  

A hands-on guide to designing and managing clinical trials, including protocol development, site management, and data reporting.  

Learn how to design a regulatory strategy for successful global submissions (FDA, EMA) throughout the drug development lifecycle.  

Deep dive into the preclinical phase of drug development focusing on safety, toxicology studies, and regulatory guidelines (ICH, GLP).