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Technical activities

  • Organisation of training sessions for the partners on good practices for medicine management: evaluation of sources (manufacturer, distributor, product), good practices for medicine storage and distribution 
  • Organisation and/or support during audits of pharmaceutical product distributors with reference to good distribution practices and the WHO's MQAS   
  • Organisation and/or support during audits of the manufacturers of finished products and manufacturers of raw materials with reference to the WHO's good manufacturing practices  
  • Evaluation and advisory services on medicine supply channels in countries where partners are operating 
  • Development of standardised tools and procedures to evaluate pharmaceutical sources and suppliers 
  • Making available to partners international standards such as pharmacopoeias, the WHO's technical reports, ICH, EU, PIC/s guidelines, etc and increasing their familiarity with them.   
  • Making an internet platform available (controlled access database) where reviewed, evaluated and verified information on medicine sources is published and updated on a regular basis.