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Regulatory affairs specialist
company • Full-time
Jun 2021 - Present • 5 yrs 4 mos
Experienced in Pharmaceutical Regulatory Affairs at (Egyptian Drug authority), with hands-on expertise in reviewing and assessing pharmaceutical registration submissions, Module 1 documentation, CPPs, and regulatory requirements. Skilled in identifying deficiencies, ensuring regulatory compliance, maintaining regulatory databases, and preparing technical committee documentation to support the pharmaceutical registration and approval process.