I am Dr. Samira Mohamadi Izad as the Qualified Person in the Nogen Pharmed Caspian nutraceutical section; I play a crucial role in safeguarding public health. My primary responsibility is to ensure the highest quality, safety, and efficacy of all medicinal products released into the market. This involves overseeing all aspects of pharmaceutical manufacturing and release, ensuring strict adherence to all relevant regulations and Good Manufacturing Practices (GMP). Ultimately, I am the final authority on the quality and release of these vital products.
As a highly motivated and results-oriented Pharmaceutical Doctorate with over 15 years of experience in the pharmaceutical industry, I possess a strong foundation in regulatory affairs, quality assurance, drug development, clinical trials. I have a deep understanding of Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and international regulatory requirements, gained through my education at Tehran University of Medical Science (TUMS). This international perspective enables me to navigate complex regulatory landscapes and ensure compliance. I am adept at effectively communicating complex scientific and technical information to diverse audiences, including regulatory agencies, internal stakeholders, and external partners, fostering collaboration and driving successful project outcomes.