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Health Sciences

Master of Pharmacy (Pharmacovigilance & Pharmacoepidemiology)

The Master of Pharmacy in Pharmacoepidemiology and Pharmacovigilance is a postgraduate programme that prepares pharmacists for advanced practice in drug safety surveillance, epidemiological research, and rational medicine use. The programme combines pharmaceutical science with epidemiological methods and pharmacovigilance practice.

Core areas include pharmacoepidemiology, pharmacovigilance, drug safety surveillance, rational medicine use, adverse drug reaction monitoring, post-marketing surveillance, research methods, and thesis. Students engage with both pharmaceutical theory and epidemiological research practice.

The programme is offered by the University of Nairobi through its Department of Pharmacy at Kenyatta National Hospital campus. This is a public university offering the programme over three academic years (six semesters) through full-time study.

Students develop competencies in pharmacoepidemiology, pharmacovigilance, drug safety monitoring, adverse drug reaction reporting, post-marketing surveillance, rational medicine use, research methods, and academic writing. The programme includes coursework, research projects, examinations, and thesis.

The University of Nairobi charges a total of KES 1,177,000 over 3 years (~KES 392,333/year): Year 1 KES 390,000, Year 2 KES 382,000, Year 3 KES 405,000. Entry requires a Bachelor of Pharmacy degree, registration with the Pharmacy and Poisons Board, and English proficiency for foreign applicants.

Graduates pursue careers as pharmacovigilance officers, pharmacoepidemiologists, drug safety specialists, regulatory affairs officers, pharmaceutical researchers, and lecturers in pharmaceutical sciences.

Skills Required

  • Pharmacoepidemiology and Drug Use Analysis
  • Pharmacovigilance and Drug Safety Surveillance
  • Adverse Drug Reaction Monitoring and Reporting
  • Post-Marketing Surveillance
  • Rational Medicine Use Promotion
  • Epidemiological Research Methods
  • Drug Safety Risk Assessment
  • Pharmaceutical Data Analysis
  • Research Methods in Pharmaceutical Sciences
  • Academic Writing and Thesis Research

Key Subjects

  • Pharmacoepidemiology
  • Pharmacovigilance and Drug Safety Surveillance
  • Adverse Drug Reaction Monitoring
  • Post-Marketing Surveillance
  • Rational Medicine Use
  • Epidemiological Research Methods
  • Drug Safety Risk Assessment
  • Pharmaceutical Data Analysis
  • Research Methods in Pharmaceutical Sciences
  • Thesis Research

Certifications

  • PPB Pharmacist Registration
  • ISPE Professional Membership

Specializations

Pharmacovigilance

Focuses on drug safety surveillance, covering adverse drug reaction monitoring, signal detection, risk management, and managing pharmacovigilance systems.

Pharmacoepidemiology

Examines drug use patterns in populations, covering epidemiological methods, drug utilisation studies, comparative effectiveness, and managing pharmacoepidemiological research.

Drug Safety and Risk Management

Covers drug safety risk assessment, covering risk identification, risk evaluation, risk minimisation, and managing drug safety risks.

Rational Medicine Use

Focuses on rational medicine use, covering drug utilisation review, prescribing audit, medication safety, and promoting rational use of medicines.

Post-Marketing Surveillance

Examines post-marketing surveillance, covering post-marketing studies, drug safety monitoring, quality surveillance, and managing post-marketing surveillance programmes.

Pharmaceutical Policy and Regulation

Covers pharmaceutical policy, covering drug policy analysis, regulatory frameworks, medicine access, and managing pharmaceutical policy and regulation.

Duration
3 years
Public, up to
Ksh 392,333
Job market
High

The programme

What you study, how long it takes, and how it is delivered.

Practicalities

Study mode
Full-time
Attachment
0 months
Average class
12 students
Award
Masters

What you study

10 subjects
  • Pharmacoepidemiology
  • Pharmacovigilance and Drug Safety Surveillance
  • Adverse Drug Reaction Monitoring
  • Post-Marketing Surveillance
  • Rational Medicine Use
  • Epidemiological Research Methods
  • Drug Safety Risk Assessment
  • Pharmaceutical Data Analysis
  • Research Methods in Pharmaceutical Sciences
  • Thesis Research

Modules

12 in the programme
  • Foundations of Pharmacoepidemiology

    Year 1Semester 14 creditsCore

    Examines pharmacoepidemiology principles, drug use patterns, epidemiological study designs, and analysing drug use in populations.

  • Pharmacovigilance Principles and Practice

    Year 1Semester 14 creditsCore

    Covers pharmacovigilance principles, adverse drug reaction monitoring, signal detection, risk management, and managing pharmacovigilance systems.

  • Adverse Drug Reaction Monitoring

    Year 1Semester 13 creditsCore

    Examines adverse drug reaction monitoring, covering ADR reporting, ADR analysis, causality assessment, and managing ADR monitoring systems.

  • Research Methods in Pharmaceutical Sciences

    Year 1Semester 23 creditsCore

    Covers research design, data collection, analysis, and conducting pharmaceutical research, preparing students for their thesis.

  • Epidemiological Study Designs

    Year 1Semester 23 creditsCore

    Covers epidemiological study designs, covering cohort studies, case-control studies, cross-sectional studies, and designing pharmacoepidemiological research.

  • Rational Medicine Use

    Year 1Semester 23 creditsCore

    Examines rational medicine use, covering drug utilisation review, prescribing audit, medication safety, and promoting rational use of medicines.

  • Post-Marketing Surveillance

    Year 2Semester 13 creditsCore

    Covers post-marketing surveillance, covering post-marketing studies, drug safety monitoring, quality surveillance, and managing post-marketing surveillance programmes.

  • Drug Safety Risk Assessment

    Year 2Semester 13 creditsCore

    Examines drug safety risk assessment, covering risk identification, risk evaluation, benefit-risk analysis, and managing drug safety risks.

  • Pharmaceutical Data Analysis

    Year 2Semester 23 creditsCore

    Covers pharmaceutical data analysis, covering statistical methods, data management, statistical software, and analysing pharmacoepidemiological data.

  • Pharmaceutical Policy and Regulation

    Year 2Semester 23 creditsCore

    Examines pharmaceutical policy, covering drug policy analysis, regulatory frameworks, medicine access, and managing pharmaceutical policy and regulation.

  • Research Seminar

    Year 3Semester 13 creditsCore

    Preparation of research proposal and thesis, including research design, literature review, methodology, and presentation.

  • Research Thesis

    Year 3Semester 210 creditsCore

    Original research thesis on a pharmacoepidemiology or pharmacovigilance topic, demonstrating mastery of research methods and pharmaceutical knowledge, assessed through written submission and oral defence.

Specialisations

  • Pharmacovigilance

    Focuses on drug safety surveillance, covering adverse drug reaction monitoring, signal detection, risk management, and managing pharmacovigilance systems.

  • Pharmacoepidemiology

    Examines drug use patterns in populations, covering epidemiological methods, drug utilisation studies, comparative effectiveness, and managing pharmacoepidemiological research.

  • Drug Safety and Risk Management

    Covers drug safety risk assessment, covering risk identification, risk evaluation, risk minimisation, and managing drug safety risks.

  • Rational Medicine Use

    Focuses on rational medicine use, covering drug utilisation review, prescribing audit, medication safety, and promoting rational use of medicines.

  • Post-Marketing Surveillance

    Examines post-marketing surveillance, covering post-marketing studies, drug safety monitoring, quality surveillance, and managing post-marketing surveillance programmes.

  • Pharmaceutical Policy and Regulation

    Covers pharmaceutical policy, covering drug policy analysis, regulatory frameworks, medicine access, and managing pharmaceutical policy and regulation.

A day as a student

A typical day during the M.Pharm in Pharmacoepidemiology and Pharmacovigilance programme combines lectures, data analysis sessions, research seminars, pharmacovigilance case discussions, and independent study. Sessions cover pharmacoepidemiology, pharmacovigilance, drug safety, rational medicine use, and research methods. Pharmacoepidemiology sessions examine drug use patterns, epidemiological study designs, and analysing drug use in populations. Pharmacovigilance sessions cover adverse drug reaction monitoring, signal detection, risk management, and managing pharmacovigilance systems. Drug safety sessions cover risk assessment, benefit-risk analysis, safety signal evaluation, and managing drug safety risks. Rational medicine use sessions cover drug utilisation review, prescribing patterns, medication safety, and promoting rational use. Research methods sessions cover epidemiological research design, data collection, statistical analysis, and conducting pharmacoepidemiological research. Data analysis sessions provide hands-on experience with pharmaceutical data analysis, statistical software, and interpreting pharmacoepidemiological data. Research seminars provide opportunities for presenting research findings, discussing current evidence, and debating pharmacoepidemiological issues. Case discussions provide practical experience with analysing adverse drug reactions, evaluating safety signals, and managing pharmacovigilance cases. Guest lectures from experienced pharmacovigilance professionals, regulatory experts, and researchers provide practical insights. The programme culminates in a research thesis on a pharmacoepidemiology or pharmacovigilance topic.

The trade offs

In its favour

  • Growing demand for pharmacovigilance professionals in Kenya with increasing drug registration and medicine access.
  • Programme is unique in Kenya, providing specialised skills in drug safety and pharmacoepidemiology.
  • Graduates are eligible for PPB pharmacist registration and ISPE professional membership, enhancing career prospects.
  • Programme has global relevance with WHO and UMC connections, providing international career opportunities.

Against it

  • Programme is expensive at ~KES 392,333/year over 3 years (total ~KES 1,177,000).
  • Only UoN confirmed offering this exact programme, limiting institutional choice.
  • Programme duration is 3 years, longer than most M.Pharm programmes.
  • Programme requires a B.Pharm degree and PPB registration, limiting access to pharmacy graduates only.

What it costs

Tuition at both ends of the market, and how to pay for it.

What it costs, and where

Against 349 health sciences courses
Public187k to 392k
187k at Moi University392k at University of Nairobi

Annual tuition in Kenyan shillings, rounded. The upright tick is the median for this field, so a bar sitting entirely to its right is an expensive programme by the standards of its own subject.

The fine print

Public: Moi 187K, UoN 392K/yr (pharmacy.uonbi.ac.ke). Private: unverified.

HELB postgraduate loans are available for Kenyan students. PPB may provide training support for pharmacy professionals. WHO may provide pharmacovigilance training support. Some pharmaceutical companies and regulatory bodies may sponsor pharmacists for postgraduate study.

Funding options

  • HELB Postgraduate Loan

  • PPB Training Support

  • WHO Pharmacovigilance Training

Scholarships

3 recorded
  • HELB Postgraduate Loan

    LoanKsh 200,000Kenyan

    Kenyan students pursuing postgraduate studies at recognised universities.

  • PPB Training Support

    ScholarshipKsh 200,000Kenyan

    Pharmacy and Poisons Board supports training and professional development for pharmacy professionals in Kenya.

  • WHO Pharmacovigilance Training

    GrantKsh 250,000

    World Health Organization provides pharmacovigilance training support for professionals in developing countries.

Getting in

The grades, the alternatives, and who accredits the award.

What you need

KCSE mean grade
N/A (Postgraduate)
Alternative entry
Applicants must hold a B.Pharm degree, be registered with PPB or equivalent regulatory body, and demonstrate English proficiency if foreign. Contact the University of Nairobi for specific admission requirements.

How you are assessed

4 components
  • Coursework and Continuous Assessment

    Coursework30% of the mark

    Continuous assessment through coursework assignments, data analysis exercises, seminar presentations, case studies, and class participation.

  • Written Examinations

    Examination40% of the mark

    Written examinations covering pharmacoepidemiology, pharmacovigilance, drug safety, rational medicine use, and research methods.

  • Practical and Research Assessment

    Practical30% of the mark

    Practical assessment through data analysis projects, pharmacovigilance case analysis, research exercises, and demonstrating pharmacoepidemiological skills.

  • Research Thesis

    Research100% of the mark

    Original research thesis on a pharmacoepidemiology or pharmacovigilance topic, demonstrating mastery of research methods and pharmaceutical knowledge, assessed through written submission and oral defence.

Accreditation

The programme is accredited by the Commission for University Education (CUE) and the Pharmacy and Poisons Board of Kenya (PPB). University of Nairobi (public) offers M.Pharm in Pharmacoepidemiology and Pharmacovigilance. The programme meets CUE and PPB standards for postgraduate pharmacy training. Graduates are eligible for PPB pharmacist registration and ISPE professional membership.

Accredited by

  • Commission for University Education (CUE)

    Academic accreditationRequired

    Programme accredited by CUE and the Pharmacy and Poisons Board of Kenya (PPB). University of Nairobi (public) offers M.Pharm in Pharmacoepidemiology and Pharmacovigilance. The programme meets CUE and PPB standards for postgraduate pharmacy training. Graduates are eligible for PPB pharmacist registration and ISPE professional membership.

Where it leads

The roles it opens, and what you leave with.

Where graduates go

6 roles
  • Pharmacovigilance Officer

    High demandKsh 200,000 to Ksh 700,000

    Manages pharmacovigilance activities in regulatory bodies or pharmaceutical companies, overseeing ADR monitoring, signal detection, and drug safety surveillance.

  • Pharmacoepidemiologist

    Moderate demandKsh 250,000 to Ksh 800,000

    Conducts pharmacoepidemiological research, overseeing study design, data analysis, and managing drug utilisation and effectiveness studies.

  • Drug Safety Specialist

    High demandKsh 250,000 to Ksh 800,000

    Manages drug safety in pharmaceutical companies, overseeing safety surveillance, risk assessment, and managing drug safety operations.

  • Regulatory Affairs Officer

    High demandKsh 200,000 to Ksh 700,000

    Manages regulatory affairs in pharmaceutical companies, overseeing drug registration, regulatory compliance, and managing regulatory submissions.

  • Pharmaceutical Researcher

    Moderate demandKsh 200,000 to Ksh 700,000

    Conducts pharmaceutical research in research institutions, producing research reports, publications, and contributing to pharmaceutical knowledge.

  • Pharmaceutical Sciences Lecturer

    Moderate demandKsh 150,000 to Ksh 600,000

    Teaches pharmaceutical sciences at university or college level, overseeing instruction, research, and academic supervision.

Graduate outcomes

Graduates pursue careers as pharmacovigilance officers, pharmacoepidemiologists, drug safety specialists, regulatory affairs officers, pharmaceutical researchers, and lecturers in pharmaceutical sciences.

Where these fields lead

8 careers

Tools you will learn

  • SPSS

    SoftwarePrimary

    Statistical analysis software for pharmacoepidemiological research, data analysis, and analysing and interpreting research data for thesis.

  • SAS

    Software

    Statistical analysis software for pharmacoepidemiology, covering advanced statistical methods, data management, and analysing large pharmaceutical datasets.

  • VigiBase

    Software

    WHO global pharmacovigilance database for accessing adverse drug reaction reports, signal detection, and managing pharmacovigilance data.

  • Stata

    Software

    Statistical software for epidemiological research, data analysis, and managing pharmacoepidemiological data analysis.

Industry links

Common misconceptions

  • Pharmacovigilance is just about reporting side effects.

    Pharmacovigilance covers comprehensive drug safety surveillance including signal detection, risk assessment, risk management, benefit-risk analysis, and post-marketing surveillance.

  • This programme is only for regulatory body staff.

    Pharmacovigilance and pharmacoepidemiology skills are valuable in pharmaceutical companies, research institutions, hospitals, and any organisation involved in drug safety and rational medicine use.

  • There is limited demand for pharmacovigilance professionals in Kenya.

    With increasing drug registration and medicine access in Kenya, demand for pharmacovigilance professionals is growing in regulatory bodies, pharmaceutical companies, and health institutions.

  • Pharmacoepidemiology is just statistics.

    Pharmacoepidemiology applies epidemiological methods to study drug use, effectiveness, and safety in populations, requiring both pharmaceutical knowledge and epidemiological skills.

  • This programme is less important than clinical pharmacy.

    Pharmacovigilance and pharmacoepidemiology are critical to public health, ensuring medicine safety and effectiveness at the population level, complementing individual patient care.

  • This programme has no practical application.

    The programme has direct practical application in drug safety monitoring, regulatory decision-making, pharmaceutical policy, and improving medicine use in health systems.

Related courses

Further reading

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