Dr. Radwa El Moneer

Dr. Radwa El Moneer is the Head of Pharmaceutical Policies & Market Access Central Administration at Egyptian Drug Authority (EDA) & also the supervisor of EDA Chairman Office.


Dr. Radwa El Moneer stands as one of the most prominent woman leaders in the field of pharmaceutical regulations in Egypt & …. Africa. Through her influential positions and dedication to improving the pharmaceutical industry, she has made significant contributions to the development and implementation of regulatory policies in the country, in a way that makes her contributions to the pharmaceutical industry in Egypt.

Dr. Reham Alassily

Reham Alassily occupies the role of Associate Director Regulatory Affairs for Near East, Middle East & Africa at IQVIA heading the regional Regulatory Affairs Hub.  Reham is armed with an extensive background of 15+ years in the field of regulatory affairs and has occupied several leading roles in key multinational companies managing wide range of portfolios (Biological, Pharmaceutical ,Consumer health and Medical devices). In her current role at IQVIA, She is supporting several companies across diverse geographics to achieve business growth via establishing solid regulatory strategies.

Ms. Naoual Assam

Biological engineer with quality control and analysis option, analysis at the national laboratory for the control of pharmaceutical products since 2013, auditor for the validation of quality control laboratories since 2016, inspector in the joint Anpp/Ministry of Commerce brigades since 2021, Currently I hold the position of technical-regulatory deputy director at the registration department of the national pharmaceutical products agency since April 2023.

Dr. Ibrahim Mustafa

Dr. Ibrahim Mustafa

Vice President of the General Authority for the Economic Zone of the Suez Canal for Investment and Promotion Affairs Since his assumption in January 2023, he has been working to achieve several goals to improve the investment environment, develop infrastructure, and increase industrial and logistical investments, by focusing on sectoral and geographical promotion.

Prior to his position, he held several positions as follows: Dr. Ibrahim Mustafa, Executive Director of Tariq Company for Economic and Financial Consultations Consultant to the first economic partnership councils in an American company and former senior advisor to the Minister of Investment Consultant to a number of local and foreign companies in the field of investment and development and an expert in economics, investment and business development – former economics lecturer for MBA students at Canadian Memorial University..

Former Senior Adviser at the Ministry of Investment and former General Coordinator of the Economic Conference (Sharm) El-Sheikh in March 2015- and a former advisor at Price Water House and Allen & Overy..- Former founding partner of Masarat Consulting. 2016-2018 Member of the Board of Directors of Collins Insurance Brokerage Company Member of the Board of Directors of Our Advisory Member of the Young Businessmen Association



Bachelor of Economics and Political Science from Cairo University 1998 Master’s degree in political economy, Cairo University, 2010 Mini Master of Business Administration accredited by Cairo University 2012


PhD in political economy

Cairo University 2021


Mr. Arthur Sichivula

Mr. Lyoko Nyambe

Dr. Donia Fady

Dr. Donia Fady is the RA Head at Takeda Pharmaceutical, Egypt

with 17+ years of experience in the pharmaceutical field, Donia has a proven track of record in regulatory strategic management utilizing strategic enterprise thinking and strong leadership skills. combining governmental and pharmaceutical companies’ experiences with strong Pharmacovigilance and QMS background.

Dr. Donia holds Bachelor’s degree of Pharmacy – Faculty of Pharmacy-Cairo university

Mr. Kent Briggs

Kent Briggs is the Managing Director at VECTOR Life Sciences. He began working with eSubmissions in 2002 and eCTDs when they were first implemented in 2003. He has provided industry workshops in the US, Canada, Europe, South Africa, India and Australia and has performed application compilation training with both big and small pharmaceutical companies around the world. In addition to performing evaluator training at over 20 health authorities, Kent has authored the eCTD specifications for 4 regions including the soon to be released specifications for ECOWAS. Since 2014, Kent has focused on the CTD in Africa and supporting the harmonization efforts through regional and continental activities.

VECTOR Life Sciences is a service provider for the African regulatory market with a key focus on the implementation and usage of electronic systems to improve regulatory efficiency. VECTOR supports customers in their transition from paper based methods to electronic processes by streamlining their regulatory operations and making their use of data more effective

Dr. Elvis Temfack

Dr. Elvis Temfack works at Africa CDC as Senior Research officer, based in Ethiopia. His background training is in clinical medicine and public health with over 15 years’ experience in clinical research and comprehensive clinical case management. Prior to joining Africa CDC, he joined Epicentre of Médecins Sans Frontières in Paris, a World Health Organization (WHO) collaborating Centre for Research in Epidemiology and Response to Emerging Diseases, working in Malawi for three years as field principal investigator generating relevant clinical evidence to support Malawian ministry of Health change pf policy for HIV first-line treatment from Efavirenz to Dolutegravir-based therapy.


He is a member of the European Society of Microbiology and Infectious Diseases (ESCMID), the International Society of Human and Animal Mycology (ISHAM) and a contributor to the Mycology One World One Guideline working group, an initiative of the European Confederation of Medical Mycologist (ECMM), ISHAM and American Society of Microbiology initiative (ASM). He has co-authored many peer reviewed publications in high readership international journals and is associate editor in some international journals. He is also a member of many collaborative working groups, serving in scientific and advisory groups addressing research in human health.

Dr. Hebal Adel

Position: Africa Cluster Manager – GSK

Lead Regulatory team for defined markets in relevant Cluster within EM organization as well as providing operational support including oversight and coordination of the operational matrix across Content Delivery, Region and Regulatory Third (3rd) Party Partners.


In my previous role within GSK Egypt, I served as Senior Regulatory Affairs manager, Planning and organizing the business goals, designing strategies to advance those goals. provide regular and constructive feedback, resolve problems and conflicts positively. Keep an eye on the regulatory environmental changes Develop effective and systemic approaches to regulatory intelligence, analyze relevant intelligence findings and communicate impact in an efficient format that facilitates awareness of business critical issues. I have a diversified experience across Pharma, Vaccine, Maintain governance and compliance, Internal control Frame work and business development.


I hold a bachelor’s degree of pharmaceutical science, a master’s degree of business administration in SMEs (Small and medium business enterprises) from the Arab Academy for Science, technology & Maritime transport.