We're proud to support our clients on their pharmacovigilance and regulatory affairs journey. Here's what they say about their experience with IntraHub Africa.
Whether you are building a new pharmacovigilance system, entering African markets, or strengthening regulatory compliance, IntraHub Africa is ready to support you.
Pharmacovigilance
ADR Reporting
Regulatory Affairs
Drug Safety
NAFDAC Compliance
Signal Detection
ICSR Management
Pharmacovigilance
ADR Reporting
Regulatory Affairs
Drug Safety
Pharmacovigilance
ADR Reporting
Regulatory Affairs
Drug Safety
NAFDAC Compliance
Signal Detection
ICSR Management
Pharmacovigilance
ADR Reporting
Regulatory Affairs
Drug Safety
African Markets Covered
At IntraHub Africa, our mission is to deliver scalable, compliant, and user-centric solutions that simplify drug safety reporting, empower stakeholders, and protect patients. We are committed to bridging the gap between pharmaceutical companies, regulatory bodies, and healthcare professionals through advanced technology and expert services.
PV system setup, ICSR case management, signal detection, and aggregate reporting aligned with NAFDAC, WHO, EMA, ICH, and FDA requirements.
Product registration, dossier preparation (CTD/eCTD), post-approval variations, GMP inspection support, and regulatory strategy across African markets.
Accredited workshops, e-learning, and certification programs in pharmacovigilance and regulatory affairs — on-site, online, or through IntraHub LMS.
Purpose-built software that replaces spreadsheets, email chains, and paper files: IntraVigi Safety Database, the IntraVigi Reporting App, PV CompliSure, and IntraHub LMS.
Compliance-driven. Technology-backed. Africa-focused. - View All Services
We focus on practical, technology-driven solutions with personalised guidance to ensure your drug safety operations are fully compliant and future-ready.
Pharmaceutical companies, CROs, and regulatory stakeholders trust IntraHub Africa across Nigeria and West Africa.
We handle end-to-end ICSR case management with full E2B(R3) compliance and regulatory submission capabilities.
With our in-depth understanding of local pharmacovigilance rules and global guidelines, you can confidently ensure compliance.
We leverage AI-driven solutions to automate ADE reporting, signal detection, and compliance, giving you the most advanced tools for drug safety.
We know your needs are unique. We focus on understanding your challenges to create tailored pharmacovigilance solutions that work for you.
We are committed to staying ahead of the curve, constantly updating our knowledge and technology to reflect the latest regulations and best practices.
Ready to modernise your PV operations? Book a Free Consultation
Enterprise PV platform: full-scale ICSR management, E2B(R3) compliance, regulatory submissions, QMS integration, and executive dashboards — built for African regulatory realities.
The public safety gateway: patients, healthcare professionals, and the public can submit ADR reports easily and securely — with AI chatbot-guided reporting flowing directly into IntraVigi Safety Database.
AI-powered PV self-assessment platform. Evaluate your PV system against requirements across multiple African countries, identify risks before inspections, and track regulatory developments.
Learning management system delivering accredited pharmacovigilance and regulatory affairs courses. Self-paced, certificate-backed, and designed around the real work African PV professionals do.
A no-obligation call to understand your products, your markets, and your current pain points. We listen first.
We review your existing PV systems, SOPs, and compliance framework — identifying gaps, quantifying risk, and documenting what needs to change.
A clear plan with timelines, deliverables, and regulatory milestones. We define scope together — no jargon, no surprises.
We build or optimise your PV system, deploy our technology platforms, train your team, and stay with you for ongoing monitoring, reporting, and audit readiness.
Let's build your pharmacovigilance system together. Book a Free Consultation
Professionals trained across West Africa through accredited workshops and our IntraHub LMS platform
Clients who partner with IntraHub Africa achieve and maintain full compliance with local and international pharmacovigilance requirements.
We're proud to support our clients on their pharmacovigilance and regulatory affairs journey. Here's what they say about their experience with IntraHub Africa.
" Before partnering with IntraHub, our PV system had significant gaps. They identified every compliance risk, built us a clear roadmap, and deployed IntraVigi seamlessly. "
" IntraHub's training programme transformed our team's understanding of pharmacovigilance. The IntraHub LMS is practical, accredited, and built around real African PV challenges. "
" PV CompliSure gave us complete visibility into our compliance posture across three markets before a scheduled NAFDAC inspection. We were fully prepared. "
Ready to strengthen your pharmacovigilance operations? Book a Free Consultation
Embark on a journey towards enhanced patient safety, reduced regulatory risk, and stronger market competitiveness — with a team built for Africa.
Safeguard patients and boost confidence in your products with reliable drug safety monitoring systems.
Achieve full compliance with local and international requirements, avoiding costly penalties and delays.
Simplify your pharmacovigilance and regulatory workflows, freeing up valuable time and resources.
Position your brand as a leader in responsible drug development and marketing across African markets.
Free initial consultation
No hidden fees or surprises
Ongoing support after implementationFind clear answers to the most common questions about our pharmacovigilance and regulatory affairs services, technology, and process.
Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. It ensures medicines on the market are continuously monitored for safety.
We work with NAFDAC, WHO, EMA, ICH, and FDA requirements. Our team stays continuously updated on local and international regulatory developments across African markets.
Yes. Our Regulatory Affairs team handles product registration, dossier preparation (CTD/eCTD), post-approval variations, and regulatory strategy specifically designed for African market entry.
We provide four purpose-built platforms: IntraVigi Safety Database (enterprise PV), IntraVigi Reporting App (public ADR reporting), PV CompliSure (AI-powered compliance assessment), and IntraHub LMS (accredited PV training).
ADR reports can be submitted through the IntraVigi Reporting App — available to patients, healthcare professionals, and the general public. Reports can be submitted manually or through our AI chatbot-guided reporting flow, and feed securely into the IntraVigi Safety Database.
Stay current with in-depth insights, emerging regulatory changes, and important drug safety updates relevant to African pharmaceutical markets.
