| المدونة | جهة الإصدار | تاريخ الإصدار | بشــأن |
|
Points to consider for setting the remaining shelf-life of medical products upon delivery |
منظمة الصحة العالمية | 2020 | Points to consider for setting the remaining shelf-life of medical products upon delivery |
|
WHO Technical Report Series, no. 1025: Good storage and distribution practices for medical products |
منظمة الصحة العالمية | 2020 | اشتراطات التخزين والتوزيع الجيد |
|
Quality management system requirements for national inspectorates |
منظمة الصحة العالمية | 2020 | Quality management system requirements for national inspectorates |
|
WHO Technical Report Series, no. 1011: Guidelines on procedures and data requirements for changes to approved biotherapeutic products |
منظمة الصحة العالمية | 2018 | دليل إجراءات ومتطلبات المتغيرات على المستحضرات الحيوية المسجلة |
|
WHO good practices for desk assessment of compliance with good manufacturing practices, good laboratory practices and good clinical practices for medical products regulatory decisions |
منظمة الصحة العالمية | 2018 | WHO good practices for desk assessment of compliance with good manufacturing practices, good laboratory practices and good clinical practices for medical products regulatory decisions |
|
WHO good manufacturing practices for the manufacture of herbal medicines |
منظمة الصحة العالمية | 2018 |
WHO good manufacturing practices for the manufacture of herbal medicines |
|
WHO good manufacturing practices for the manufacture of herbal medicines |
منظمة الصحة العالمية | 2018 |
WHO good manufacturing practices for the manufacture of herbal medicines |
|
WHO guidance on good manufacturing practices: Model inspection report |
منظمة الصحة العالمية | 2016 |
WHO guidance on good manufacturing practices: Model inspection report |
|
WHO Technical Report Series, no. 993: Guidelines on procedures and data requirements for changes to approved vaccines |
منظمة الصحة العالمية | 2015 | دليل إجراءات ومتطلبات المتغيرات على اللقاحات المسجلة |
|
General guidance on hold-time studies
|
منظمة الصحة العالمية | 2015 | General guidance on hold-time studies |
|
Technical supplements to Model guidance for the storage and transport of time- and temperature–sensitive pharmaceutical products |
منظمة الصحة العالمية | 2015 | Technical supplements to Model guidance for the storage and transport of time- and temperature–sensitive pharmaceutical products |
|
WHO Technical Report Series, no. 992: TRS 992 Annex 9 Good review practices: guidelines for national and regional regulatory authorities |
منظمة الصحة العالمية | 2015 | دليل ممارسات المراجعة الجيدة |
|
WHO good manufacturing practices for pharmaceutical products: Main principles |
منظمة الصحة العالمية | 2014 | WHO good manufacturing practices for pharmaceutical products: Main principles |
|
WHO guidelines for drafting a site master file
|
منظمة الصحة العالمية | 2011 | WHO guidelines for drafting a site master file |
|
Model guidance for the storage and transport of time and temperature sensitive pharmaceutical products |
منظمة الصحة العالمية | 2011 |
Model guidance for the storage and transport of time and temperature sensitive pharmaceutical products |
|
WHO good manufacturing practices for sterile pharmaceutical products |
منظمة الصحة العالمية | 2011 | WHO good manufacturing practices for sterile pharmaceutical products |
|
WHO good manufacturing practices for active pharmaceutical ingredients (bulk drug substances) |
منظمة الصحة العالمية | 2010 | WHO good manufacturing practices for active pharmaceutical ingredients (bulk drug substances) |
|
WHO good manufacturing practices for pharmaceutical products containing hazardous substances |
منظمة الصحة العالمية | 2010 | WHO good manufacturing practices for pharmaceutical products containing hazardous substances |
|
WHO good manufacturing practices for the manufacture of pharmaceutical excipients |
منظمة الصحة العالمية | 1999 | WHO good manufacturing practices for the manufacture of pharmaceutical excipients |
|
WHO – guideline for safe disposal of unwanted pharmaceutical |
منظمة الصحة العالمية | 1999 |
مدونة منظمة الصحة العالمية لطرق الاعدام الآمن الخاصة بالمستحضرات الصيدلية |
|
Inspection of pharmaceutical manufacturers |
منظمة الصحة العالمية | 1992 |
Inspection of pharmaceutical manufacturers |
|
WHO- management of waste from immunization campaign activities guideline |
منظمة الصحة العالمية | 2004 |
مدونة منظمة الصحة العالمية بشأن كيفية إدارة المخلفات الناتجة عن حملات التطعيم |
|
WHO guidelines on pre-approval inspections
|
منظمة الصحة العالمية | 2002 |
WHO guidelines on pre-approval inspections |
| الدليل الإرشادى الخاص بوزارة البيئة بشأن إدارة نفايات الرعاية الصحية فى مصر. | وزارة البيئة المصرية | 2015 | إدارة نفايات الرعاية الصحية فى مصر |
عفواً , الموقع لا يدعم هذا المتصفح