At Crown College of Canada, I completed a mock e-CTD submission project for an antipsychotic drug, using CTD Modules 1–5.
I applied FDA, Health Canada, ICH, and GMP requirements relevant to pharmaceutical product registration. For the project, I prepared manufacturing process descriptions, facility and equipment documentation, stability summaries, and quality risk assessments.
My MSc in Regulatory Affairs – Clinical Research at Northeastern University included a capstone on a mock New Drug Administration (NDA) e-CTD submission. I also hold a BSc (Hons) in Biomedical Science from Northumbria University.
In patient-facing and customer-facing roles, I maintained records and supported compliance with documentation requirements. At TurboTax, Intuit, I guided customers through tax software and documented interactions; at Toronto Heart & Health Women's Clinic, I maintained patient records and coordinated follow-ups.
