Anthony Toroitich

Background

About Anthony Toroitich

Skilled pharmaceutical industry professional with a strong academic background in public health and extensive experience especially in pharmaceutical regulatory affairs for low-and middle-income countries (LMICs). I have a deep desire to improve access to essential quality, safe and effective medicines and biologics, and medical devices primarily to the LMICs for better health. I am a quality assessor with World Health Organization, Prequalification Program with good experience in pharmaceutical quality assurance systems strengthening and management. Seasoned leader and manager with good interpersonal relations and able to take up new assignments quickly and adapt to new environments. Over time have built long-term strategic partnerships and relationships with donors, health system actors, regulatory authorities, key decision-making stakeholders, and influencers in Health. My thought process is always out-of-the-box with new ideas that produce tangible solutions to health challenges encountered in low-middle income countries. Dedicated, passionate, and delivered results on time and within budget in a value-based organization with a focus on empowerment, teamwork, motivation, and mentorship to others. My areas of expertise include: • Harmonization of technical standards and guidelines as a Certified Quality Management Systems Auditor East African Community and Intergovernmental Authority on Development. • Management of communities of practice and technical partnerships • Development of sound multi-country technical donor proposals • Implementation, monitoring, and evaluation of multi-country project activities and work plans • Pharmaceutical Product Registration: Dossier review, Product Information, Post-Approval Changes/Variations for major regulatory agencies across Sub Sahara Africa and World Health Organization prequalification of medicines program. Review. • Good Manufacturing Practice (WHO cGMP) Auditor/Inspector for Pharmaceutical Products. • Pharmaceutical Product Development, Product Management and Marketing, Product Supply, Quality Assurance, Internal Controls, and Market Access for generic medicines and biosimilar medicines.