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
Not sure where to start?

Book a free 30-minute discovery call and leave with clear next steps.
Book a consultation →
Who we help
About
FAQ
Contact

Book a consultation

Services

Training that builds in-house capability

Pharmacovigilance and regulatory affairs training for your staff, online or at your premises.

Book a training enquiry See what’s included

Training

What’s included

Pharmacovigilance training

Practical pharmacovigilance training for your staff, online or at your premises.

Regulatory affairs training

Practical regulatory affairs training for registration and lifecycle teams.

What you receive

A course tailored to your products
Course materials for your team
Certificates of attendance

How it runs

Training FAQ

Yes, in person in Eldoret and across Kenya and the region, or online.

Training that builds in-house capability

Book a training enquiry