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Hamada Sherif

Chairman associate for updating & developing registration systems & general manager for human drug registration Egyptian Drug Authority (EDA)

Hamada Sherif is the general director for the general administration for registration of human pharmaceutical drugs at the Egyptian Drug Authority (EDA), where being responsible for the market authorization of new registration & re-registration of human pharmaceutical drugs.

Hamada started his career as a quality control analyst almost 17 years ago in the national organization for drug control (NODCAR) & research after graduation from faculty of pharmacy Cairo university with grade excellent with honour, in 2010 started the new career path as a registration specialist also in NODCAR.

In 2020 with establishment of EDA Started a new career as the general manager for the technical support in the quality control laboratories until June 2022 where promoted to the current title in EDA as the general director for the general administration for registration of human pharmaceutical drugs.

See Hamada Sherif at this event

  • Day 2 Wednesday 4 December

Reliance across the product life cycle: PACs & GMPs

Session objectives:

  • Discuss how reliance can be implemented for PACs and what tools are available to streamline reliance in this area.
  • Highlight findings from literature, industry surveys and available data to illustrate the complexity of the current global PACs framework.
  • Address challenges and propose solutions to further implement reliance for GMP inspections.

Speakers