Pharmaceutical Regulatory Affairs: Open Access

R Zaki

Publications

• Research Article
  Pharmaceutical Good Manufacturing Practice Regulatory Affairs in Sudan: Continuous Debate between Regulatory Authority and Manufacturers
  Author(s): Abubaker Abdellah, M I Noordin, R Zaki and Ali AbedallahAbubaker Abdellah, M I Noordin, R Zaki and Ali Abedallah
  
  Background: The implementation of GMP requirements in Sudan as developing country imposes pressure on both the manufacturers and regulatory authorities since resources are limited and additional regulatory and manufacturing facilities are required. Objective: The study aimed to assess the regulatory affairs of pharmaceutical good manufacturing practice in Sudan. Method: A structured questionnaire was given to the secretary general of the Sudanese National Medicines and Poisons Board (NMPB). Other different questionnaire was conducted to get information from manufacturers. The study questionnaire .. Read More»
  DOI: 10.4172/2167-7689.1000166

  Abstract PDF