Mr. Hilton Tommy Stevens
Mr. Hilton Tommy Stevens has been with PSI (Population Services International) South Africa, an American based Medical Devices and Pharmaceutical Social Business, as the Head of the Regulatory Affairs and Quality Assurance. This role is responsible for the oversight and coordination of product registration and quality compliance for Sub-Saharan Africa regions. Currently also supporting New […]
Dr. Marie Bouchra
Dr. Marie Bouchra is Regulatory Professional with sixteen years of experience in Regulatory Affairs and over a decade of experience in the African Regulatory landscape, started her career with Johnson and Johnson in 2009, held various roles of increasing responsibilities. Currently Regional Manager Regulatory Affairs and Policy for Middle East and Africa, specializing in advancing […]
Dr. Mona Al Moussli
Dr. Mona Al Moussli is the Co-Founder and Managing Director of PRA Consultancy, with over 20 years of expertise in pharmaceutical and medical device regulatory affairs. She has led key initiatives like the GCC RA Pharma Summit and the AfriSummit and developed the GCC Regulatory Affairs Course. Dr. Al Moussli also serves on several advisory boards, contributing to healthcare advancement […]
Mr. Erik Vollebregt
Mr. Erik specialises in EU legal and regulatory frameworks for medical devices, digital health technologies, pharmaceuticals, and life sciences, with distinctive expertise in AI, software, in vitro diagnostics and personal data protection. As a multilingual legal expert with extensive experience at the European Commission and several leading international law firms, he provides strategic counsel on […]
Dr. Rana Chalhoub
Dr. Rana Chalhoub is an experienced Regulatory Affairs Professional with a demonstrated history of working in leading multinational medical devices companies such as Medtronic, Johnson & Johnson and Hospira Pfizer. During her career, Rana has managed to take over regulatory roles of increased responsibilities with an extended area coverage where she has built extensive knowledge […]
Dr. Karim Wahba
Dr. Karim Wahba is the Head of Regulatory Affairs and Trade Compliance for Middle East & Africa at Merck life science. With over 13 years of experience within regulatory management in medical device, life science and FMCG industries, Karim is a seasoned expert in navigating complex regulatory landscapes and ensuring compliance with international regulations. His […]
Mr. Marc Chaillou
Mr. Marc Chaillou is Head of Sales at Schlafender Hase. He has been working for the Pharmaceutical & Medical Devices industries for the last 13 years. Marc specialises in Regulatory Labelling and specifically how processes & technologies can reinforce, or compromise patient safety.
Mr. Bill McMoil
Mr. Bill McMoil joined RAPS in 2017 as Chief Operating Officer and has served as Executive Director since April 2020. Since joining RAPS, McMoil has grown the organization from 26,000 to 35,000 members globally; staff from 40 to 60; and annual revenue by 57%. By expanding RAPS portfolio of products and services, he has championed […]
H.E. Dr. Hisham Stait
Dr. Hisham Stait has been serving as the Chairman of the Unified Procurement Authority (UPA), Egypt, since 2025. Prior to this role, he was the Vice Chairman of UPA since 2020, overseeing supply chain management for Egypt’s governmental healthcare sector, ensuring the procurement and distribution of essential medical supplies across the entire healthcare spectrum. His […]
Mr. Rowland Sefakor
Mr. Rowland Sefakor is the Head of the Medical Devices Department at the Food and Drugs Authority, Ghana. With over ten (10) years of experience in medical devices analysis, he has been instrumental in helping the medical devices laboratory achieve accreditation to ISO 17025 in eight (8) scopes, including sampling by attributes according to ISO […]