Veeresh Babu Pratap
Teaching
Hyderabad
Regulatory Affairs Specialist (ADDRA-Certified) with Ph.D. in Pharmacology and hands-on expertise in CTD/eCTD dossier preparation, global guidelines (USFDA, EMA, ICH, CDSCO), and pharmacovigilance. Proven in regulatory strategy, lifecycle management, and compliance from advanced diploma training; complemented by pharmacology research (65+ publications) and teaching (guest lectures on regulatory affairs). Transitioning from academia to industry to deliver high-quality submissions and intelligence-driven compliance.
Regulatory Tools: CTD/eCTD, Dossier Preparation, Pharmacovigilance, Drug Approval Processes
Guidelines: USFDA, EMA, ICH, CDSCO