Senior Regulatory Executive
Shabnam Hussain
Scientific Writing
Delhi, India
5 Years
Joined May 2026
Global Regulatory And Consumer Insights
Drug Regulatory Department
0 Consultations
About me
Prepare, author, review comprehensive clinical study reports and study protocols. Analyze data from clinical trials regulatory submissions. Conduct scientific writing and editing of clinical and regulatory documents, Investigator’s Brochures (IBs), Chemistry, Manufacturing, and Controls documentation, IND ,knowledge and working familiarity with guidelines and submission requirements of health authorities, CDSCO, USFDA, and EMA, ensuring all documentation meets regional and global compliance.
Skills
RegulatoryClinical TrialCTRI RegistrationComplianceMS office
My Services
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