Regulatory Affairs Expert
Specializing in MENA regulation, medical devices EU MDR 2017/745, FDA submissions, and Biosimilars
About me
Independent consultant supporting companies with regulatory and business solutions across pharmaceuticals, medical devices, and life sciences sectors. My services are focused on enabling market access, regulatory compliance, and quality alignment with business goals.
Your Path To Innovation
What Services I’m Providing
Regulatory review, evaluation & submission; Generic, medical devices, EU MDR 2017/745, QMS & ISO 13485.
Gap analysis, technical documentation, CTD/eCTD submissions, and CE marking
Business development, market entry strategies, managing audits, and identifying growth opportunities in emerging markets
Training courses in regulatory frameworks in MENA, sterile generics, medical devices EU MDR 2017/745.