Jael Morangi
Qualified Person for Pharmacovigilance (QPPV)
Pharmacovigilance Expert | Patient Safety Advocate | Regulatory Compliance Specialist
About Jael
Jael Morangi is a highly experienced Qualified Person for Pharmacovigilance (QPPV) with a deep commitment to patient safety and pharmaceutical excellence. With over a decade of experience in the pharmaceutical industry, Jael has developed comprehensive expertise in pharmacovigilance systems, adverse drug reaction monitoring, and regulatory compliance.
As a registered QPPV with the Pharmacy and Poisons Board (PPB) of Kenya, Jael plays a crucial role in ensuring that pharmaceutical companies meet their regulatory obligations while maintaining the highest standards of patient safety. Her work encompasses the entire spectrum of pharmacovigilance activities, from system design and implementation to ongoing monitoring and regulatory reporting.
Beyond her pharmacovigilance expertise, Jael is the proprietor of Sadima Pharmacy, a community pharmacy based in Kahawa Wendani. This hands-on experience in pharmacy operations provides her with invaluable practical insights into real-world pharmaceutical challenges and patient care, enriching her approach to pharmacovigilance consulting.
Jael's approach to pharmacovigilance is characterized by a practical, hands-on methodology that combines technical expertise with a deep understanding of the Kenyan regulatory landscape. She works closely with pharmaceutical companies to build robust PV systems that are not only compliant but also sustainable and effective in protecting public health.
Areas of Expertise
Comprehensive pharmacovigilance services tailored to the Kenyan market
PV System Setup & Implementation
Design and implementation of comprehensive pharmacovigilance systems from scratch, including SOPs, processes, and documentation frameworks.
QPPV Nomination & Regulatory Compliance
Expert guidance on QPPV nomination processes, PPB registration, and ongoing regulatory compliance requirements.
ADR Reporting & Signal Detection
Comprehensive adverse drug reaction case management, assessment, reporting to regulatory authorities, and proactive signal detection.
PV Training & Capacity Building
Customized training programs for pharmaceutical teams on PV principles, ADR identification, regulatory requirements, and best practices.
PV Audits & Gap Analysis
Thorough audits of existing pharmacovigilance systems to identify compliance gaps and provide actionable improvement recommendations.
Risk Management Planning
Development and implementation of risk management plans, including risk minimization strategies and periodic safety update reports (PSURs).
Professional Qualifications & Certifications
Qualified Person for Pharmacovigilance (QPPV)
Registered with the Pharmacy and Poisons Board (PPB) of Kenya as a qualified person responsible for pharmacovigilance activities.
Pharmaceutical Sciences Background
Strong foundation in pharmaceutical sciences with specialized training in drug safety and pharmacovigilance principles.
Regulatory Compliance Expertise
In-depth knowledge of PPB regulations, WHO guidelines, and international pharmacovigilance standards including ICH guidelines.
Work With Jael
Get expert pharmacovigilance support to ensure your compliance and protect patient safety
How Jael Can Help Your Organization
Urgent: PPB QPPV Nomination Deadline - December 31, 2025
Don't risk regulatory action. Get expert help with your QPPV nomination today.
Commitment to Patient Safety
"My mission is to help pharmaceutical companies in Kenya build robust pharmacovigilance systems that not only meet regulatory requirements but truly protect patient safety. Every adverse event reported and every safety signal detected contributes to safer healthcare for all Kenyans."
- Jael Morangi, QPPV