
Every medicine we make is built on quality. From carefully selected materials and validated processes to rigorous in‑process controls and final release testing, we apply strict standards at every step. Our teams work in line with global good manufacturing and quality practices, supported by continuous improvement and ongoing monitoring, so patients and healthcare professionals can rely on consistent safety, efficacy, and performance.

“Our dedication to uncompromising quality emphasizes our responsibility to empower health as a human right.”
Dr. Manal Hamdy
Global Integrated Compliance Governance Director
European medicines agency (EMA), Egyptian Drug Authority (EDA), Saudi FDA (SFDA), GCC regulators, National Agency for Food and Drug Administration and Control (NAFDAC), Tanzania Bureau of standards (TBS), as well as the Board of Pharmacy and Poisons - Kenya.
EVA Pharma’s facilities are entirely accredited according to several global standards; Our Quality Management Systems are certified by ISO 9001:2015 & ISO 13485:2016 for Medical devices. Our Global Compliance team is accredited in Inspection activities by ISO/IEC 17020:2012 from PJLA to ensure compliance over different facilities. Eventually, we have been qualified and endorsed by well-known regulatory authorities worldwide.
We empower the fight for health and well being as a human right.
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For adverse events reporting, please contact us on
PV.Report@evapharma.com