Pharmaceutical industry in Africa set to automate compliance through partnership between Infinity Health and IntraHub
Infinity Health Africa and IntraHub Africa Partner to Transform Pharmaceutical Regulation in Africa
Infinity Health Africa and IntraHub Africa have joined forces to revolutionize regulatory compliance and pharmacovigilance in the African pharmaceutical sector. Their goal is to help pharmaceutical companies enhance the quality and rigor of their regulatory documentation, improve readiness for Good Manufacturing Practice (GMP) certification, and simplify tracking and analysis of adverse drug reactions (ADR), thereby strengthening patient safety systems across the continent.
The partnership seeks to address longstanding regulatory challenges in Africa by digitizing and automating compliance processes, supporting local and international regulatory audits, building advanced pharmacovigilance systems, and promoting regulatory excellence at every stage of pharmaceutical operations.
IntraHub Africa, a pharmacovigilance service provider, offers the IntraVigiTM platform, which enables drugmakers and health providers to track adverse drug reactions, maintain safety reports, and comply with international pharmacovigilance standards. On the other hand, Infinity Health Africa's proprietary platform ONBOARD manages product registration, licensing, and post-marketing surveillance. Together, they position themselves to shape a more rigorous and tech-enabled regulatory environment for pharmaceutical companies across Africa.
Pharm. Abubakar Mukhtar, CEO of IntraHub Africa, stated that the partnership brings together expertise, technology, and a shared vision to help companies thrive and keep patients safe. This collaboration also aims to enable African pharmaceutical companies to compete globally while ensuring patient safety and building trust within Africa's healthcare ecosystem.
The African pharmaceutical market is projected to grow to $70 billion by 2030, and with tightening regulations across the continent, the need for robust compliance tools is more crucial than ever. Nigeria's NAFDAC, for instance, now requires mandatory bioequivalence studies for all generic drugs submitted for registration.
This partnership comes at an opportune time as the Moonshot event by the website is scheduled in Lagos on October 15-16, offering a platform for Africa's top founders, creatives, and tech leaders to network and share future-forward ideas.
With a cumulative experience managing over 200 regulatory submissions, their combined expertise and technology-driven approach position them to lead a digital transformation in regulatory compliance and drug safety that promotes sustainable growth and better health outcomes across Africa's pharmaceutical industry.
[1] Infinity Health Africa and IntraHub Africa Press Release, [Link to Press Release] [2] Pharmaceutical Technology Africa, "Infinity Health Africa and IntraHub Africa Partner to Transform Pharmaceutical Regulation in Africa", [Link to Article]
- The partnership between Infinity Health Africa and IntraHub Africa aims to revolutionize regulatory compliance in the African pharmaceutical sector.
- Their goal is to help pharmaceutical companies ensure the quality and rigor of their regulatory documentation.
- The partnership seeks to simplify tracking and analysis of adverse drug reactions (ADR) to strengthen patient safety systems.
- The aim is to improve readiness for Good Manufacturing Practice (GMP) certification.
- The partnership intends to digitize and automate compliance processes.
- IntraHub Africa offers the IntraVigiTM platform for tracking adverse drug reactions and maintaining safety reports.
- Infinity Health Africa's ONBOARD platform manages product registration, licensing, and post-marketing surveillance.
- Together, they aim to shape a more rigorous and tech-enabled regulatory environment.
- The collaborative effort brings together expertise, technology, and a shared vision.
- This partnership aims to enable African pharmaceutical companies to compete globally while ensuring patient safety.
- The African pharmaceutical market is projected to grow to $70 billion by 2030.
- With tightening regulations across the continent, the need for robust compliance tools is more crucial than ever.
- Nigeria's NAFDAC now requires mandatory bioequivalence studies for all generic drugs submitted for registration.
- The Moonshot event by a website is scheduled in Lagos, offering a platform for future-forward ideas.
- The combined expertise and technology-driven approach position them to lead a digital transformation.
- This transformation promotes sustainable growth and better health outcomes across Africa's pharmaceutical industry.
- The partnership's stated goal is to help companies thrive and keep patients safe.
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