Evanjo is a Cairo-based CRO providing Phase I-IV clinical trial services across MENA and Africa, including clinical monitoring, site and project management, medical device trials (Class IIa/IIb/III and AIMD), medical writing, data management, biostatistics, pharmacovigilance and regulatory affairs. Their regulatory team handles CTA submissions to authorities including Egypt CAPA, Saudi FDA (SFDA), UAE MoHAP and South Africa SAHPRA. A medical supplies arm also represents Egyptian manufacturers for global export.
Vendor description
Best suited for sponsors seeking regional full-service coverage or regulatory entry into Egypt and wider MENA / Africa markets, where local authority relationships and ICH-GCP compliance matter more than global scale.
Programmes needing MENA / Africa regional coverage, CTA submissions to local authorities, or medical device trials in the region
- Regional regulatory expertise across MENA and Africa (Egypt CAPA, SFDA, UAE MoHAP, SAHPRA CTA submissions)
- Full-service scope: clinical operations, medical writing, data management, biostatistics, pharmacovigilance
- Medical device and diagnostics trial experience (Class IIa, IIb, III and AIMD)
- Medical supplies arm supports regional trial logistics and sourcing
- Small regional provider with limited public track record and no published study counts
- No public employee-review footprint located
- MENA / Africa focus — not a fit for programmes needing a US / EU regulatory lead
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Review snapshot
No public employee-review footprint located for Evanjo.
No consistent public positive themes located
No consistent public negative themes located
Insufficient public evidence
Pricing
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Key facts
| HQ country | Egypt |
|---|---|
| Geography | MENA / Africa |
| Service model | Full Service CRO |
| Customer segment | mixed |
| Study phases | Phase I, Phase II, Phase III, Phase IV |
| Trial scale | Regional MENA / Africa programmes |
| Therapeutic areas | Generalist |
| Last reviewed | 2026-08-18 |
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