The Egyptian Drug Authority (EDA) announced the conclusion of a workshop titled “The Third Edition of the Regulatory Guide for the Review and Evaluation of Analytical Files of Human Pharmaceutical Products.”

The workshop aimed to enhance industry partners’ awareness of the approved work mechanisms within the Central Administration for Pharmaceutical Control, and to clarify the content of the third edition of the regulatory guide related to the review and evaluation of analytical files for human pharmaceutical products. This contributes to ensuring the quality and safety of pharmaceutical products and medical supplies, and to improving the efficiency of regulatory procedures in line with the latest international standards and best practices.

This comes as part of the Authority’s ongoing efforts to develop work mechanisms and elevate the level of services in accordance with the latest global standards and good practices, reaffirming the quality, safety, and availability of pharmaceutical products and medical supplies.