Heba Hashem

Heba has been working with Regulatory Affairs in the Middle East for more than 25 years. She has a Pharmaceutical and Business background being a graduate of the Faculty of Pharmacy (Cairo University), RAC certified in addition to an MBA at Maastricht School of Business. For the past 20 years Heba held the position of Middle East & Africa Regulatory and Quality Head at different Pharmaceutical and Medical Device companies; Gambro, Bayer and Novo Nordisk.

Heba is now the Middle East and Africa Associate Director at PPD where she is providing regulatory consulting services and training to Health Care companies.

  • Next: 10-14 Jun 2024 Live online

Global Pharmaceutical Regulatory Affairs Summer School

Summer school

Live online

Unlock the world of pharmaceutical regulatory excellence with our Global Pharmaceutical Regulatory Affairs training – an intensive journey through the diverse regions, offering practical insights, expert guidance, and strategic mastery for professionals seeking to navigate and succeed in the dynamic global regulatory landscape.

  • 84 CPD hours
  • Presented by Heba Hashem
  • Next: 11-12 Jun 2024 Live online
  • Also: 7-8 Oct 2024 Live online

Medical Device Regulations in the Middle East and North Africa

Live online

This seminar will provide an essential overview of the key areas of requirements for product approvals for medical devices in the Middle East and North Africa. Covering Algeria, Bahrain, Egypt, Israel, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Saudi Arabia, Sudan, Syria, Tunisia, UAE and Yemen

  • 12 CPD hours Focused
  • Presented by Heba Hashem
  • Next: 22-23 Apr 2024 Live online
  • Also: 26-27 Jun 2024 Live online
  • Also: 9-10 Dec 2024 Live online

Pharmaceutical Regulatory Affairs in the Middle East

Live online

Covering Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Palestine, Qatar, Saudi Arabia, Sudan, Syria, UAE and Yemen

  • 12 CPD hours Focused
  • Presented by Heba Hashem