A named qualified person for pharmacovigilance, adverse event reporting to the Pharmacy and Poisons Board, periodic safety reports and safety signal management.
Product registration with the Pharmacy and Poisons Board and other East African regulators, dossiers, variations, renewals and local representation.
Pharmacovigilance audits, inspection readiness and written procedures that reflect how your team really works.
A medical information service that answers questions about your products and captures adverse events.
Pharmacovigilance and regulatory affairs training for your staff, online or at your premises.
Advice on entering the Kenyan and East African markets and keeping up with regulatory changes.
Book a free 30-minute discovery call and leave with clear next steps.
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PVRA SOLUTIONS
PVRA SOLUTIONS