Enhance Your Compliance Skills: Online Pharma Training in the Middle East
Join our comprehensive online training on pharmaceutical regulatory affairs in the Middle East to excel in market access and compliance.
Overview of the Training Course
An upcoming online training session on pharmaceutical regulatory affairs is set for April 12-13, 2027. This two-day program is designed for industry professionals eager to deepen their understanding of regulatory compliance and expedite market access in the Middle East.
Who Will Benefit?
This training is especially pertinent for individuals who work closely with regulatory departments or are involved in the preparation of submission documents and commercial planning in the region. It's also ideal for those aiming to strengthen their foothold in Middle Eastern pharmaceutical markets or adapt to continually updating regulatory landscapes.
What You Will Learn
- Recognize critical regulatory disparities across the Middle East.
- Navigate submission expectations successfully.
- Understand the trajectory of regional regulatory harmonization.
Participants will enhance their skill set to support registration processes and tailor strategies to meet dynamic market demands effectively.
CPD Credit Hours
The training grants 12 CPD hours, enabling attendees to earn professional development points while expanding their knowledge base.
Target Audience
This course is tailored for:
- Regulatory affairs professionals operating within the Middle East.
- Individuals newly introduced to the region, including roles in Regulatory Affairs, Pharmacovigilance, Market Access, and Business Development.
- Anyone seeking updates on recent regulatory developments in the pharmaceutical landscape.
Meet the Instructors
Ilona Putz
Ilona Putz, the founder and General Manager of PULONA Emerging Markets, is based in the UAE and has been pioneering regulatory consultancy solutions for international healthcare manufacturers since 2008. With a career in the pharmaceutical industry stretching back to 1988, she has worked with major companies like MSD and Sandoz. Ilona is recognized for her contributions to discussions on clinical trials and has published several articles in professional journals.
Heba Hashem
Heba Hashem brings over 25 years of regulatory affairs experience in the Middle East, backed by her educational credentials from Cairo University and Maastricht School of Business. She has held key positions in various pharmaceutical and medical device companies, focusing on regulatory and quality standards. Currently, Heba serves as the Associate Director at PPD, offering regulatory consulting and training services.
Learn More
For more details about this enriching training opportunity, visit ResearchAndMarkets.com.
About ResearchAndMarkets.com
ResearchAndMarkets.com stands as the premier source for global market research reports and data. The platform provides comprehensive insights into regional markets, key industries, and the latest trends affecting the pharmaceutical sector.