Ishan Nadeeka
Ampara, Sri Lanka
I am ishan nadeeka, a verry talented writer
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About Me
am a Clinical Research & Regulatory Affairs Specialist with 2years of experience in medical writing, regulatory submissions, and clinical trial documentation. My expertise includes preparing eCTD submissions, clinical study reports, investigator brochures, protocols, and regulatory documents aligned with FDA, EMA, and ICH guidelines.
I specialize in medical & scientific content development, literature reviews, and regulatory compliance for pharmaceuticals, medical devices, and biotechnology. My goal is to deliver accurate, well structured, and high quality documentation that meets regulatory standards and supports successful approvals.
With a strong background in clinical trials and regulatory submissions, I ensure clarity, precision, and compliance in every project. Let’s collaborate to achieve regulatory success and scientific excellence in your projects!
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