Our Consultants
LEARN MORE ABOUT OUR CONSULTANTS
Dr. Mohammad Salah
GMP Compliance Manager, Rotabiogen Pharmaceutical Industries
Dr. Mohammad is a seasoned GMP professional with a strong foundation in pharmaceutical GMP and a deep understanding of national and international regulatory requirements, having previously held the position of Deputy Manager, Pharmaceutical Industry Development Unit, at the Egyptian Drug Authority (EDA). He brings 12 years of invaluable experience from the Inspection department of the EDA, where he honed his expertise in conducting rigorous GMP inspections, assessing compliance, and ensuring the safety and quality of pharmaceutical products.
Within EDA, he participated in pharmaceutical factories certification committees as a GMP expert. He also was one of the independent reviewiers of conducted inspections reports and was responsible for delivering advanced GMP training.
Dr. Mohammad is a seasoned GMP professional with a strong foundation in pharmaceutical GMP and a deep understanding of national and international regulatory requirements, having previously held the position of Deputy Manager, Pharmaceutical Industry Development Unit, at the Egyptian Drug Authority (EDA). He brings 12 years of invaluable experience from the Inspection department of the EDA, where he honed his expertise in conducting rigorous GMP inspections, assessing compliance, and ensuring the safety and quality of pharmaceutical products.
Within EDA, he participated in pharmaceutical factories certification committees as a GMP expert. He also was one of the independent reviewiers of conducted inspections reports and was responsible for delivering advanced GMP training.
Dr. Amany Al Tanany, PhD
Technical Director and Deputy CEO at UPharma (EFG Hermes Group).
Dr. Amany is a highly distinguished professional with over 22 years of experience in the pharmaceutical industry. Her expertise in GMP, Quality Management, and Regulatory Affairs was honed during her tenure at the Egyptian Drug Authority (EDA). As a member of the Layouts Review/Approval Committee, she gained invaluable insights into the critical aspects of pharmaceutical facility design and compliance. She also served as Head of Raw Materials, Food Supplements and Follow-Up Inspection Departments.
Dr. Amany is currently pursuing a doctoral degree in Strategic and Quality Management from the Arab Academy for Science, Technology & Maritime Transport (commenced in 2022).
She holds a Master’s degree in Pharmaceutical Business Administration from the Faculty of Pharmacy, Suez Canal University.
Dr. Amany is a highly distinguished professional with over 22 years of experience in the pharmaceutical industry. Her expertise in GMP, Quality Management, and Regulatory Affairs was honed during her tenure at the Egyptian Drug Authority (EDA). As a member of the Layouts Review/Approval Committee, she gained invaluable insights into the critical aspects of pharmaceutical facility design and compliance. She also served as Head of Raw Materials, Food Supplements and Follow-Up Inspection Departments.
Dr. Amany is currently pursuing a doctoral degree in Strategic and Quality Management from the Arab Academy for Science, Technology & Maritime Transport (commenced in 2022).
She holds a Master’s degree in Pharmaceutical Business Administration from the Faculty of Pharmacy, Suez Canal University.
Dr. Mahmoud Sa’eed
Dr. Mahmoud is a recognized leader in the field of Good Manufacturing Practices (GMP) for pharmaceuticals. He is the former Head of the Pharmaceutical Industry Development Unit and previously held head of inspection follow‐Up section at the Egyptian Drug Authority. Throughout his distinguished 15-year career at the Egyptian Drug Authority, he has played a pivotal role in developing and implementing new GMP regulations, conducting inspections, assessing GMP adherence and fostering industry-wide compliance.
Within EDA, he also served as a member of the Drug Factories Licensing Committee, a member of Track and Trace Project Committee and was responsible for technical GMP training and qualification programs.
Within EDA, he also served as a member of the Drug Factories Licensing Committee, a member of Track and Trace Project Committee and was responsible for technical GMP training and qualification programs.
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