Ms. Diana Diaz Guzman
Ms. Diana Diaz is a highly experienced and passionate professional dedicated to strengthening global healthcare ecosystems to ensure access to safe, quality-assured medicines. She is a Senior Regulatory Intelligence Manager at the United States Pharmacopeia (USP), and a Regulatory System Strengthening (RSS) consultant for the World Health Organization (WHO). With over 15 years of experience in regulatory affairs and 10 years of […]
Ms. Evelyn Aseawa Paintsil
Ms. Evelyn A. Paintsil is a Regulatory Officer with the Food and Drugs Authority (FDA), Ghana, where she currently serves as the Acting Unit Head for the Fast Track and Low Risk Unit within the Drugs and Nutraceuticals Department. In this role, she oversees the evaluation of product dossiers for medicines and leads the training […]
Mr. Marwan Zeidan
Mr. Marwan Zeidan is leading EVOTEQ’s business development and client relationships, responsible to drive growth while maintaining client satisfaction. He has over 25 years of rich experience that has encompassed various disciplines in business development, sales and delivery across complex IT/OT digital solutions, public sector offerings, and smart buildings/cities. Prior to joining EVOTEQ, he was […]
Dr. Omnia Ayman
Dr. Omnia Ayman is the Manager of the Biological Protocols Unit and GCP Inspector at the Egyptian Drug Authority (EDA). She specializes in clinical research regulation and in the evaluation of preclinical studies and clinical trials involving biologicals, biosimilars, and vaccines. She also conducts Good Clinical Practice (GCP) inspections at clinical trial sites and relevant […]
Dr. Neveen Kamel
Dr. Neveen holds a degree of Bachelor of Pharmacy – Faculty of Pharmacy – Cairo University, She is currently Head of Regulatory Affairs North Africa, Egypt, French Speaking Africa & Scientific Office Manager of Merck Egypt, supporting regulatory policy advocacy efforts for the region. She has 25 years of experience in industry and 20 […]
Dr. May Badran
Dr. May have over 18 years of experience in pharmaceutical industry , dedicated pharmacist specializing in regulatory affairs field . She has got a proven track record of ensuring compliance with industry regulations and guidelines in Emerging markets to support the registration and access to medications. Her current role is Regulatory Director in Abbott for […]
Mr. Asif Alavi
Mr. Asif Alavi is the General Manager for North Africa at Haleon. He brings a rich and diverse commercial leadership experience spanning more than 25 years across different geographies. In Haleon for the past 14 years, Mr. Asif started off as Sales Head for the Pakistan business before moving to Arabia as Sales Director. He […]
Dr. Amal Fathy
Dr. Amal Fathy has over 15 years of experience in the pharmaceutical industry. Her career journey is diverse, having held various roles starting in Sales, then moving into Sales Force Effectiveness, and later transitioning into Regulatory Affairs — where she discovered her true passion. She has since advanced in her career, managing all functions within […]
Mr. Varma Bhupathiraju
Mr. Varma Bhupathiraju is the Associate Vice President – Global Regulatory Affairs at Biocon Biologics Limited. With over 23 years of experience in the biopharmaceutical industry, Varma Bhupathiraju is a recognized leader in global regulatory affairs, specializing in the development and approval of biologics. He has played a pivotal role in securing approvals for multiple biological products, […]
Mr. Raja Sekhar Vanga
Mr. Raja Sekhar Vanga is the Vice President – Global Regulatory Affairs at Biocon Biologics Limited. With over 25 years of experience in the Biopharmaceutical Industry, he is a thought leader in regulatory affairs, specializing in the development and global registration of more than ten biosimilar products. He has successfully navigated complex regulatory landscapes to secure approvals […]