Our commitment to innovation and continuous improvement is evident in our substantial investments in R&D labs. Our skilled team conducts lab-scale trials, scale-up activities, and troubleshooting for production and stability issues. We establish batch records, evaluate initial batches, and develop protocols for Quality Assurance. Our R&D team ensures cutting-edge performance and competitiveness in a rapidly evolving industry. 

EIPICO is dedicated to maintaining exceptional quality standards through its rigorous Quality Control (QC) department. We prioritize adherence to GMP guidelines, employing cutting-edge technology and upholding the latest pharmacopoeial references. Our comprehensive testing covers all stages, from raw materials to finished products, ensuring their safety and efficacy. With internationally accredited microbiology labs, stability studies, and water analysis, we demonstrate our commitment to excellence. 

 As EIPICO is one of the Pioneers in the Pharmaceutical Industry in Egypt, Middle east, and Africa, Quality assurance is of paramount importance in EIPICO.
As quality means continuous improvement as well as consistency, Eipico invested a lot in improving the quality level by upgrading all systems and adding new technologies to meet the requirements of GMP in order to ensure the consistent production of safe and effective medication.
Eipico have a lot of GMP certificates from different authorities , you can find Eipico on Eudra GMP Data base , WHO prequalification program , MHRA Database and many other world wide authorities which reflects the high level of our quality system.
Quality assurance apply the standard procedures and adhere to the regulations of GMP. We pride ourselves in having a robust Quality System with a compendious set of harmonized processes and procedures.
These include providing integrated medical safety evaluations and benefit-risk assessments as well as monitoring the quality and safety of in-market and investigational products.