Patient safety first
Every report, dossier and decision starts from the patient who will take the product.
About us
Patient safety and regulatory clarity, from Eldoret to East Africa
PVRA Solutions helps pharmaceutical, medical device and health product companies register products, run compliant pharmacovigilance systems and stay ready for regulators across East Africa.
Our story
Why PVRA exists
PVRA stands for Pharmacovigilance and Regulatory Affairs: the two disciplines that decide whether a medicine reaches patients, and whether it stays safe once it does.
We started PVRA Solutions in Eldoret to give manufacturers, importers and distributors a partner who knows both disciplines and the regulators that apply them. Instead of one consultant for the dossier, another for safety reporting and a third for audits, our clients work with one team that carries their product from registration to routine post-market surveillance.
Our work is practical. We write procedures people actually follow, prepare dossiers that answer the questions regulators ask, and stay available when an inspection, a safety signal or a variation needs a fast response.
How we work
What clients can expect from us
Right first time
Submissions checked against current guidance before they reach the regulator.
One named lead
A single accountable contact for your team and for the regulator.
Confidential by default
Work under NDA, need-to-know access and the Kenya Data Protection Act 2019.
FAQ
About working with us
In Eldoret, Kenya. We work with clients and regulators across Kenya and East Africa, online and in person.
Yes, before any documents are shared.
After a free discovery call we send a written proposal with scope, timeline and fees. Nothing is paid online.
Talk to a regulatory expert this week.
A free 30-minute discovery call. No obligation, clear next steps.