Joelle Blok

Regulatory Affairs & Pharmacovigilance Director META

Professional Overview
Joelle Blok is an accomplished Regulatory Affairs and Pharmacovigilance professional with over 15 years of experience in the pharmaceutical industry. As the Regulatory Affairs & Pharmacovigilance Director for the META (Middle East, Turkey, and Africa) region at Acino, she is responsible for providing strategic leadership and driving compliance within a diverse portfolio of pharmaceutical products.

Experience Summary

Current Role
In her current role as Regulatory Affairs & Pharmacovigilance Director META at Acino, Joelle oversees all regulatory and pharmacovigilance activities across the region. She is responsible for ensuring the timely and compliant registration of new products, managing post-approval changes, and maintaining robust pharmacovigilance systems to monitor the safety of Acino's medications. Joelle's expertise and proactive approach have contributed to Acino's successful market expansion and regulatory compliance in the META region.

Career Progression
Prior to her current role, Joelle held progressive positions in regulatory affairs and pharmacovigilance at Astellas Pharma and Pharmachemie B.V. She has extensive experience in navigating complex regional regulatory environments, having worked across the MENA, GCC, and SSA (Sub-Saharan Africa) markets. Joelle's proven track record in leading cross-functional teams, implementing effective compliance strategies, and driving successful product registrations has positioned her as a respected industry leader.

Academic Background
Joelle holds a Bachelor's degree in Pharmacy from the University of Utrecht in the Netherlands. Her academic background, combined with her extensive industry experience, has equipped her with a deep understanding of pharmaceutical regulations, quality assurance, and product safety.

Areas of Expertise

• Regulatory affairs and compliance management

• Pharmacovigilance and safety monitoring

• Product registration and lifecycle management

• Cross-functional team leadership and collaboration

• Strategic planning and project management

• Navigating diverse regulatory environments in the META region

Professional Impact
During her career, Joelle has successfully registered numerous pharmaceutical products in various markets, contributing to the expansion of her employer's portfolios. Her expertise in regulatory affairs and pharmacovigilance has been instrumental in ensuring the timely and compliant introduction of innovative therapies, ultimately improving patient access to essential medicines. Joelle's leadership and commitment to excellence have earned her a reputation as a trusted adviser and a valuable asset to the organizations she has served.

Conclusion
Joelle Blok's extensive experience, technical expertise, and strategic leadership make her a valuable asset in the pharmaceutical industry. As the Regulatory Affairs & Pharmacovigilance Director META at Acino, she continues to drive regulatory compliance and product safety, contributing to the company's growth and patient-centric mission in the region.