About Qeema Egypt

Providing technical excellence in pharmaceutical validation, engineering, and compliance.

Our Founding Story

QEEMA Egypt was established in the 10th of Ramadan City, Egypt, as a specialized consulting firm to meet the growing need for high-quality, scientifically sound validation and qualification services in the pharmaceutical sector. We realized that local drug manufacturers faced complex regulatory hurdles while attempting to align with international frameworks like the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA).

By combining specialized engineering with deep pharmaceutical quality knowledge, QEEMA has grown into a highly trusted partner, assisting dozens of factories in design qualification, cleanroom air balancing, thermal mapping, and QMS implementation.

Why Our Experience Matters

We don't provide general industrial advice. Our consultants are pharmaceutical specialists who spend their days inside sterile cleanrooms, testing HVAC systems, calibrating autoclaves, mapping warehouses, and writing Validation Master Plans. We understand both the theory and the hard science behind Good Manufacturing Practice (GMP).

Our Team Credentials

  • ISO Lead Auditors: Certified ISO 9001, ISO 14001, and ISO 45001 auditors to ensure your internal QMS and safety policies match global standards.
  • GMP Diplomas & Training: Continuous validation education in EU GMP Annex 1 requirements, aseptic simulations, and computer system validation (GAMP 5).
  • Professional Memberships: Active networking and knowledge exchange with leading global pharmaceutical engineering institutions (ISPE and PDA).

Our Mission

To empower pharmaceutical and healthcare manufacturers in Egypt and the MENA region to achieve absolute compliance with local EDA guidelines and international GMP expectations through precise engineering and validation.

Our Vision

To be the primary technical authority and validation partner for sterile and non-sterile pharmaceutical manufacturers in the Middle East and Africa, recognized for scientific precision and regulatory integrity.

Our Values

Precision in measurement, transparency in audit findings, scientific integrity, compliance-driven design, and dedicated support for the pharmaceutical manufacturer's journey.

Leadership Team

Meet the leaders driving technical validation and regulatory compliance at Qeema.

Dr. Mahmoud Ayad
Dr. Mahmoud Ayad
Technical Director & GMP Consultant

With over 14 years in pharmaceutical engineering, Dr. Mahmoud is an expert in sterile validation, HVAC qualification, sterilization validation (steam, dry heat), and EU GMP compliance audits.

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Dr. Amany Tanany
Dr. Amany Tanany
CEO & QMS Consultant

Dr. Amany specializes in Quality Management System design, SOP drafting, sterile manufacturing operations, documentation management, and preparative audits for local EDA license launches.

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