Dr. Fouad H. Darras Graduated with a PhD in medicinal chemistry from Regensburg University in Germany (2014) and a master’s degree in intellectual property rights (LL.M) from the University of Turin- Department of Law in Italy (2016); the program was jointly organized by the International Training Center of the International Labor Organization (ITCILO) and The World Intellectual Property Organization (WIPO).


Liliana Teles is a pharmacist holding a Master in Pharmaceutical Sciences and a Master in Pharmaceutical Medicine.


Specialized in Regulatory Affairs, Product Development and Quality Assurance for the cosmetics industry, she is a certified EU Cosmetics Safety Assessor with a Post-Graduation in Advanced Cosmetology.


As Regulatory Affairs Manager at Critical Catalyst – Health Consulting, Liliana works closely with manufacturers, importers and distributors of cosmetics and medical devices located worldwide to ensure compliance with EU regulations and safe access to the EU market.



Dr. Noha El Hariri is the general manager of the general medical device registration administration-Egyptian drug authority (EDA).


She had Bachelor of Clinical Pharmacy year 2003 with excellent grade with honor.

She had MBA (Master of Business Administration in health economics) with grade excellent with honor.


She worked in the central administration for pharmaceutical affairs since 2004 as inspector

In 2011 she left the inspection department and joined the medical device department since 2011.


In 2013 she became head of variation department in medical devices unit.

In 2020 she became general manager of registration department.


She is a Clinical pharmacist that graduated from Jordan University on 2011 – Pharm. D

Previously, she was a clinical pharmacist at king Hussein Cancer Centre from 2011 till 2018.


Dr. Rand has been a Regulatory affair Specialist at Jordan Food & Drug Administration (JFDA) since 2018.


In addition, she is an active member in post approval change for originator drugs committee and an active member in obligation committee.


Nazila is an aesthetic industry leader, specialized in strategic pillars of commercial, marketing, and medical education. Leading operations from launch phase to growth strategies for established businesses for Fortune 500 global aesthetic companies across 30 countries and 3 continents.


With over 17 years of experience in the healthcare industry, Nazila has advanced the aesthetic footprint of the region vis a vis geographic expansion and commercial excellence.


Nazila has curated and executed over 100 first in class medical education programs both virtually and physically cultivating speakers through mentorship and delivering cadaveric, hands on and live events. Her expertise brings together the world’s leading international speakers in medical training to the forefront of educational advancement.


Nazila has established her Aesthetic consulting agency in London and Dubai, pioneering future technologies intertwined with medical aesthetics creating a launchpad for emerging markets and products.


Dr. Marian Anwar, is Benefit Risk & Therapeutic Area Lead, Middle East & Africa, at Abbvie pharmaceutical company.


Dr. Marian is a strategic and accomplished leader with more than 15 years of resounding success in Pharmacovigilance, Clinical Research, Medical affairs and Business Development within the Pharmaceutical industry across the Middle East and Africa region. Distinguished career reflects scientific expertise in promoting the safe use of pharmaceutical products through PV system development, product vigilance, and risk assessment/mitigation strategies.


Dr. Marian started her career as a medical representative in Cairo, Egypt and then relocated to Dubai, UAE , where she held several regional senior roles in different top multinational pharmaceutical companies.


Dr. Marian accomplished Extensive knowledge of Pharmacovigilance regulations and practices in the assigned territories with profound experience in quality control and management of PV procedures with high level of collaboration with relevant stakeholders. Recognized as a Subject Matter Expert with track record of success in providing PV insights through safety assessments, regulatory compliance, PV partnership and drug safety audits.

Mr. Hussain A. Aziz Jaffar


Dr. Shatha Al-Quraan has a MSc in pharmaceutical science and a BCs in pharmacy Doctor.

She is a Co-Chair of medical device technical committee, an expert in medical device & drug registration regulations and the Former head of scientific advice section for the JFDA.

In her current role with Jordan Federal Drug Authority as the Head of medical devices registration Dept.

She Leads her team with confidence creating procedures and processes to streamline registrations for more advance treatment options for her country.


Monir El Azzouzi is a Medical Device Expert specialised in Quality and Regulatory affairs. He has worked for multiple Medical Device company where he acquired 15 years of experience. Within his experience he had to develop Quality and Regulatory affairs departments, obtain CE marking for Medical Devices, register products all over the world, deal with audits as Management Representative.



He has now created Easy Medical Device to support Medical Device companies that need help to place compliant products in the Market. He also educates the Medical Device community through his Blog, Podcast and Youtube channel. By educating everyone, we prevent issues to happen.


His motto “Would I give this product to a member of my family”. This helps him to take decisions.


RIMA NSHEIWAT is a pharmacist with 17 years of experience in regulatory activities in both pharma and Para-pharma industry.


Through her career in the Arab Drugstore-Jordan, she successfully established and managed different operational departments such as supply chain, quality compliance, in addition to regulatory and intelligence department, which gave her enrichment exposure to registration experience from different perspectives.


Moreover, she was part of the teams responsible for revision of different JFDA regulations, member in drug owner association, in addition to her active participation in many workshops and conferences as speaker and participant.


Recently and as a regional director for regulatory and intelligence at AMSA BV (Amsterdam Medical & Scientific Alliance), she is handling a holistic market access activities with different stakeholders covering pharma and non-pharma healthcare industry.


Her passion and dedication, along with her two master degrees (Public health and MBA), supported her remarkable achievements in different regulatory scopes.