Jeyflex Pharmacovigilance Services Across Africa

Is Your Pharmacovigilance System Ready for Its Next Inspection?

Adverse event backlogs, QPPV gaps, and missed PSUR deadlines put your products and your market access at risk. Jeyflex manages the full pharmacovigilance lifecycle for pharmaceutical companies across Africa, so your compliance never becomes a liability.

The Real Cost of Getting PV Wrong

Pharmacovigilance failures rarely announce themselves until it’s too late — a missed signal, a late PSUR, an inspection finding that could have been caught months earlier. If any of this sounds familiar, you are not alone:

Your QPPV role has been vacant, understaffed, or stretched too thin across markets
Adverse event case processing is falling behind, creating regulatory exposure
You are unsure whether your PSMF would withstand an NMRA audit today
Signal detection is reactive rather than proactive, leaving risks unmanaged for too long
You need local PV representation in an African market but have no presence there

Jeyflex exists to close exactly these gaps — with hands-on, practitioner-led pharmacovigilance support across 16 African markets.

Medical device vigilance, as known as materiovigilance, is the collection, assessment, reporting and identification of trends in incidents resulting from the use of medical devices.

Why Pharmaceutical Companies Choose Jeyflex

Four reasons pharmaceutical companies across Africa trust Jeyflex with their pharmacovigilance obligations.

Pan-African Coverage

One PV partner managing your safety obligations across 16 African markets — instead of juggling multiple separate local contacts.

ISO 9001:2015 Certified

Our quality management systems are independently certified, so your PSMF and case files are always audit-ready.

Full Lifecycle Expertise

From QPPV provision to signal management to PSUR authoring, we cover the complete PV lifecycle under one roof.

Practitioner-Led, Not Just Theoretical

Our team has processed live cases and sat through real NMRA inspections — hands-on experience, not just policy knowledge.

Explore Our Pharmacovigilance Services

Each category below links to a dedicated service page with full details on scope, deliverables, and how Jeyflex’s approach addresses that specific compliance need.

Pharmacovigilance Regulatory Compliance

Stay continuously compliant with global and African PV regulations — without scrambling before every audit.

Risk Management & Signal Detection

Catch safety signals before they become regulatory findings.

Quality Assurance & Audits

Build a PV quality system that passes inspection the first time.

Medical Information Management

Never let a medical information query go unanswered or untracked.

Training & Consultancy

Equip your team or let us manage day-to-day case operations for you.

Comprehensive Pharmacovigilance Services

Explore our range of pharmacovigilance services tailored to every phase of your product’s life cycle.

Pharmacovigilance by Life Cycle

Covering every phase from product development to post-market surveillance.

QPPV & Local Safety Officer

Dedicated QPPV, LPPV, and Local Safety Officer services for seamless compliance and oversight.

Literature Monitoring

Stay updated with safety signals across global and regional African publications continuously.

Safety Database Management

Efficient management of safety databases with comprehensive management services.

Medical Devices & IVD Vigilance

Post-market surveillance for medical devices and in-vitro diagnostics across African markets.

Pharmacovigilance Training

Equip your team with the knowledge and skills through customized GVP and PV training programmes.

Pharmacovigilance Across 16 African Markets

Pharmacovigilance in Africa requires more than a generic global playbook. Each market has its own regulatory authority, reporting requirements, and local representation rules. Jeyflex provides dedicated, on-the-ground PV support across East Africa, West Africa, North Africa, and Southern Africa.

🌍 East Africa

Kenya

PPB · Full PV operations

Uganda

NDA · Case management

Ethiopia

EFDA · PV system setup

Flag of Rwanda.svg

Rwanda

RFDA · Safety monitoring

Tanzania

TMDA · Audit & reporting

🌍 West Africa

🇳🇬 Nigeria

NAFDAC · Full PV support

🇬🇭 Ghana

FDA Ghana · PV compliance

🇸🇳 Senegal

DPM · Safety reporting

🇧🇫 Burkina Faso

LNSP · PV support

🇬🇲 Gambia

MHRA Gambia · Compliance

🇨🇮 Ivory Coast

DPM · ADR reporting

🇬🇦 Gabon

ANPGM · PV compliance

🌍 North Africa & Southern Africa

🇪🇬 Egypt

EDA · PV operations

🇹🇳 Tunisia

DPHM · Safety compliance

🇿🇦 South Africa

SAHPRA · Full PV support

Interested In Our Pharmacovigilance Services?

Fill the form below and we’ll get back to you as soon as possible. Please provide as many details as necessary to help us serve you better. Thank you for considering working with us.

Frequently Asked Questions

Frequently asked questions about Jeyflex pharmacovigilance services.

A Qualified Person for Pharmacovigilance (QPPV) is the individual legally responsible for overseeing a company’s pharmacovigilance system in a given market — including case processing, signal management, and regulatory reporting. Jeyflex provides QPPV and Local QPPV services across East Africa.

Yes — outsourcing PV to a specialised, ISO-certified provider like Jeyflex is a widely accepted and compliant model used by pharmaceutical companies globally, provided the provider has documented SOPs, a robust PSMF, and audit-ready systems, all of which Jeyflex maintains.

Yes. One of Jeyflex’s core strengths is managing unified PV portfolios across Kenya, Uganda, Tanzania, Rwanda, and Ethiopia from a single point of contact — simplifying reporting and reducing the overhead of coordinating multiple local vendors.

Onboarding timelines depend on the size of your existing case backlog and the maturity of your current PSMF, but Jeyflex typically begins with a system audit to identify priority gaps, followed by a phased handover — ensuring no compliance gap during the transition.

Pharmaceutical Compliance Solutions for Algeria