The Egyptian Drug Authority (EDA) announced the conclusion of the sixth round of the training program titled: "A Comprehensive Overview of Common Technical Document (CTD) Modules and Standards for File Preparation and Submission." The program was organized by the Authority in cooperation with the Chamber of Pharmaceutical, Medical Supplies, and Cosmetics Industry, concluding on February 1, 2026.

The program aimed to support the Chamber’s member companies by training work teams responsible for registration and quality files on the Common Technical Document (CTD) system. This joint initiative seeks to improve the efficiency of preparing, reviewing, and submitting technical registration files, thereby enhancing the capabilities and skills of registration and quality managers within these companies.

The program's activities included discussions on several key topics, most notably:

Comprehensive CTD Overview: Providing a detailed look at all modules of the Common Technical Document.

Regulatory Standards: Reviewing the specific standards governing the preparation and submission of registration files.

Capacity Building: Engaging with trainees from various companies operating in the sector to ensure practical application of these standards.

This comes as part of the Egyptian Drug Authority's commitment to supporting and developing the pharmaceutical industry and boosting investments in this vital sector.