Pharmacovigilance
A named qualified person for pharmacovigilance, adverse event reporting to the Pharmacy and Poisons Board, periodic safety reports and safety signal management.
Regulatory Affairs
Product registration with the Pharmacy and Poisons Board and other East African regulators, dossiers, variations, renewals and local representation.
Quality & Compliance
Pharmacovigilance audits, inspection readiness and written procedures that reflect how your team really works.
Medical Information
A medical information service that answers questions about your products and captures adverse events.
- Medical information service
- Adverse event intake
Training
Pharmacovigilance and regulatory affairs training for your staff, online or at your premises.
- Pharmacovigilance training
- Regulatory affairs training
Market Access & Advisory
Advice on entering the Kenyan and East African markets and keeping up with regulatory changes.
- Market entry advice
- Regulatory updates and intelligence
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Services

Medical information handled properly

Medical information and adverse event intake lines staffed by trained professionals.

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Medical Information

What’s included

Medical information service

Trained professionals answering medical questions about your products.

Adverse event intake

Adverse event reports received, documented and passed into case processing.

What you receive

Documented responses to medical enquiries
Adverse events passed into case processing
Monthly activity reports

How it runs

Medical Information FAQ

Yes. Any adverse event mentioned in an enquiry is documented and passed into case processing.

Medical information handled properly

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