Training Program: International Design Requirements for Pharmaceutical & Medical Device Industries per GMP

2026-01-15General Authority for Industrial Development — CairoPharmaceutical & Medical Devices Industries
Register / Contact usContact form

Summary

Dr. Mamdouh Soliman, EIG's Managing Director, delivered a specialized training program on the design requirements for pharmaceutical and medical device facilities per Good Manufacturing Practices (GMP), and was honored by Dr. Nahed Youssef, Chairperson of the General Authority for Industrial Development.

Highlights

Driven by its commitment to supporting and advancing the industrial sector in Egypt, Egyptian International Group – EIG for Consultancy organized and delivered a specialized training program by Dr. Mamdouh Soliman, the Group's Managing Director, entitled: "International Design Requirements for Pharmaceutical & Medical Devices in Light of Good Manufacturing Practices (GMP) & International Quality Standards." The program highlighted the latest global requirements for the design of pharmaceutical and medical device manufacturing facilities in alignment with GMP and international quality frameworks, supporting the competitiveness and global readiness of Egyptian industry. Dr. Nahed Youssef, Chairperson of the General Authority for Industrial Development, honored Dr. Mamdouh Soliman in recognition of his dedicated efforts and his valuable scientific and practical contributions in supporting and advancing the industrial sector in line with international standards. #GMP #Good_Manufacturing_Practices #International_Standards #Pharmaceutical_Design #Quality #Medical_Devices #GAHAR

Schedule & Venue

Date

2026-01-15

Venue

General Authority for Industrial Development — Cairo

Want to attend our next event or run a similar program for your team?

Reach out to EIG to reserve your seat in upcoming events or design a tailored program for your organization.

Chat on WhatsAppSend a message