john magdi

• Revision & Selection of Trade Names for new drug applications.
• Revision of outer & inner labels of pharmaceutical drugs.

• Community pharmacies (Local Market) follow up.
• Governmentally supplied drugs (MOH Tender) Follow up.
• Important pharmacological groups and drug categories (CVS, CNS, Biological products, Life-saving drugs, etc.) follow up by monthly monitoring distributors' stocks and monitoring production & packaging at the manufacturers, to prevent shortages that may take place and take strict & immediate actions in case of sudden shortages.
• Receiving public complaints about drugs in short (via hot-line, written official letters, e-mails) and working on solving those complaints.
• Manufacturers and Importers support to solve their CAPA related problems that lead to drug shortages.
• Reporting urgent and complicated drug shortages issues to decision makers.
• Issuing Periodical drug shortages bulletin.
• Predict and therefore prevent the occurrence of any shortages.

• Preparing soft and hard registration dossiers for imported and local products (pharmaceutical, cosmetics, food supplement and disinfectants)
• following up all the stages of registration with the Competent governmental authorities till obtaining the registration licenses
• Cooperate and communicate with the different competent authorities due to a long fruitful relationship with most of governmental authorized stuff in the following places.
• Submitting and issuing of the import plans and permits from the competent authorities
• Following up the final release of pharmaceuticals.
• Making suggestions to improve the performance by identifying the areas that need enhancement and ways to achieve that.
• Making suggestions for new product submissions.
• Collect data and prepare submissions to regulatory agencies
• Identifies trendsetter ideas by researching industry and related events, publications, and announcements; tracking individual contributors and their accomplishments.
• Locates or proposes potential business deals by contacting potential partners; discovering and exploring opportunities.
• Screens potential business deals by analyzing market strategies, deal requirements, potential, and financials; evaluating options; resolving internal priorities; recommending equity investments.
• Develops negotiating strategies and positions by studying integration of new venture with company strategies and operations; examining risks and potentials; estimating partners' needs and goals.
• Closes new business deals by coordinating requirements; developing and negotiating contracts; integrating contract requirements with business operations.
• Enhances organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.

• Providing different studies and policy analyses needed for decision making, policy formulation, necessary regulations development and their implantations.
• Provide technical assistance for development, implementation and monitoring of national medicines policy and strategic plan.
• Provide technical and decision support to different departments to solve problems and simplify procedures for better responsiveness to clients.
• Formulated the new pharmaceutical policy that addressed the emerging challenges in the pharmaceutical field on the regional and international level.
• Reviewed and implemented the new regulatory framework including registration, pricing, supply chain and importation regulations.
• Studied and analyzed issues and documents referred by the head of CAPA and presented recommendations.

• Preparing issues referred by companies for presenting on technical committee, including issues from all departments at CAPA.
• Reception &Evaluation of the New Human Drug Applications.
• Data entry for the new application.
• Revise and manage the data base for the registered human drug
• Sharing in the legislation and implementation of the new regulations and decrees at the current time