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Good Pharmacovigilance Practices Training

Master Drug Safety with Industry-Leading (GVP) Certification

Advance your career in drug safety with our comprehensive 12-week Good Pharmacovigilance Practices (GVP) Certification. Designed for pharmacovigilance professionals, healthcare practitioners, and aspiring pharmaceutical specialists, this hybrid course delivers practical, globally-aligned training that equips you to protect public health while meeting WHO, EMA, and FDA compliance standards.

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Pharmacovigilance Training

Program Details

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Duration

  • Duration: 6 weeks (2 lessons per week, 2 hours per session – 24 contact hours)

  • Delivery Mode: Virtual with interactive case studies and discussions.
    First session is hybrid (physical attendance encouraged for networking).

Requirements & Assessment

  • Prerequisite: Basic pharmacology or healthcare knowledge recommended.
    (Supplementary materials provided)

  • Assessment: Quizzes, assignments, and final evaluation.
    (70% pass rate required for certification)

Investement

  • Cost: Ksh 30,000 (exclusive of VAT)

  • Pre-registration Fee: Ksh 4,200

  • Balance: Payable within the first week of training

Why This Training is Essential

In today’s rapidly evolving pharmaceutical landscape, the stakes for drug safety have never been higher. Organizations face mounting pressure to prevent adverse drug reactions, maintain regulatory compliance across multiple jurisdictions, and respond swiftly to emerging safety signals. Without structured, industry-aligned training in Good Pharmacovigilance Practices, professionals risk compliance failures, career stagnation, and crucial forfeitures to make meaningful contributions to patient safety.

Where many professionals struggle;

Complex global regulatory frameworks Spanning WHO, EMA, and FDA standards that require specialized knowledge to navigate effectively

Insufficient practical experience in critical areas like Risk Management Plans (RMPs), signal detection, and adverse reaction reporting

The knowledge gap between theoretical pharmacology training and real-world pharmacovigilance application.

Evolving technologies including AI-driven safety monitoring that demand continuous upskilling.

Career limitations due to lack of recognized certification and specialized drug safety expertise.

What You Will Master in This Program

This certification program transforms you into a confident, competent pharmacovigilance professional equipped to handle the full spectrum of drug safety challenges. Through our practical, case-based curriculum, you will:

  • Master global regulatory frameworks and legal requirements governing pharmacovigilance across WHO, EMA, and FDA jurisdictions
  • Develop comprehensive Risk Management Plans (RMPs) that proactively identify and mitigate drug safety concerns
  • Navigate adverse reaction reporting systems with confidence, including specialized areas like vaccine and medical device vigilance
  • Implement quality management systems and prepare Pharmacovigilance System Master Files (PSMFs) to industry standards
  • Identify and evaluate safety signals using evidence-based methodologies and communicate findings effectively to stakeholders
  • Apply ethical frameworks to complex drug safety decision-making scenarios
  • Leverage emerging technologies including AI applications in pharmacovigilance to future-proof your skillset
  • Build interpersonal and emotional intelligence skills that enhance your effectiveness in cross-functional safety teams
  • Understand entrepreneurial applications of pharmacovigilance that drive organizational success and innovation
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Who Should Attend This Program

Pharmacovigilance Professionals

Seeking to deepen expertise and ensure compliance with evolving global standards

Healthcare Practitioners

Looking to specialize in drug safety monitoring and adverse event management

Regulatory Affairs Specialists

Requiring comprehensive pharmacovigilance knowledge for compliance roles

Quality Assurance Professionals

In pharmaceutical manufacturing and distribution

Clinical Research Associates

Transitioning into drug safety careers

Pharmacy Graduates and Students

Eager to enter the pharmaceutical industry with a competitive advantage

Medical Affairs Teams

Responsible for safety surveillance and benefit-risk assessment

Pharmaceutical Companies

Seeking to upskill teams in GVP compliance and best practices

Course Curriculum

Module 1: Introduction to Pharmacovigilance

Establish your foundation with legal frameworks, ethical principles, and an overview of global pharmacovigilance regulations and their practical application.

Module 2: Pharmacovigilance Systems

Explore quality management principles, audit processes, and master the development and maintenance of the Pharmacovigilance System Master File (PSMF).

Module 3: Risk Management & Reporting

Learn to develop effective Risk Management Plans (RMPs) and master the full spectrum of adverse reaction reporting, including specialized areas such as vaccine vigilance and medical device safety monitoring.

Module 4: Signal Detection & Safety Communication

Develop skills to identify potential safety signals from diverse data sources and communicate findings effectively to regulatory authorities, healthcare professionals, and other key stakeholders.

Module 5: Entrepreneurial Insights & Future Trends

Discover how pharmacovigilance creates organizational value, explore business applications of drug safety, and prepare for emerging trends including artificial intelligence in pharmacovigilance.

Our Faculty

Learn from industry experts with extensive experience in pharmacovigilance and regulatory affairs

Dr Jerusha Kamau

Lead Trainer | CEO, Jeyflex Consultants Ltd.

Dr. Jerusha is a pharmaceutical compliance expert and the CEO of Jeyflex Consultants Ltd, a Nairobi-based firm dedicated to advancing healthcare standards through specialized consulting. With over a decade of expertise in pharmacovigilance, regulatory affairs, and capacity building, she empowers professionals to navigate complex regulatory landscapes and strengthen patient safety. Beyond her role at Jeyflex, Dr. Kamau serves as Director for the Healthcare Sector at GS1 East Africa, driving innovative track-and-trace solutions for medical products. Currently authoring the Pharmaceutical Regulatory Handbook, she is a thought leader committed to shaping the future of pharmaceutical compliance across the region.

Program Details

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Duration

6 weeks (2 lesson per week, 2 hours per session, 24 contact hours)

Delivery Mode

Virtual with interactive case studies and discussions; first session hybrid (physical attendance encouraged for networking).

Prerequisite

Basic pharmacology/healthcare knowledge recommended (supplementary materials provided).

Assesment

Quizzes, assignments, and a final evaluation (70% pass rate for certification).

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Investment

Cost

Ksh 30,000 (exclusive of VAT)

Pre-registration fee

Ksh 4,200

Balance payable within the first week of training.

Secure Your Future in Drug Safety Enroll Today

Take advantage of our limited-time introductory offer and position yourself at the forefront of pharmaceutical safety. With only a few spots remaining at the special rate of Ksh 25,000 (regular price Ksh 30,000), now is the time to invest in your professional development.

Ready to get started? Complete the enrollment form below to reserve your spot in the November 1st cohort. Have questions? Contact us at +254 798 725 500 or [email protected].