A.    Approval of Clinical Trials in Lebanon

This section has been developed for individuals and organizations involved in health-related research with human participants. In particular, this document is intended to provide guidance to design and carry out health research studies to provide guidance on the requirements of the Lebanese Ministry of Public Health to approve a clinical trial in Lebanon.

 

B.    Authorization of Institutional Review Boards (IRBs)/Research Ethics Commitees (RECs)

This section has been developed to give guidance to hospitals and universities who have their own IRBs/RECs on the requirements needed by the Lebanese Ministry of Public Health to be officially authorized to be allowed to review and oversee the ethical aspects of research that involve human subjects. Hospitals and centers who do not have their own IRBs/RECs are allowed to be affiliated with authorized IRBs/RECs per the requirements of the Ministry.

 

 

C.     Exportation of Biological Samples as part of clinical trials

This section is developed to give guidance to researchers and sponsors who wish to export biological samples (blood, urine, etc) to be tested outside the country as part of clinical trials protocols on the requirements needed to obtain the approval from the ministry.

 

 

د. السجل اللبناني للتجارب السريرية (LBCTR)

السجل اللبناني للتجارب السريرية (LBCTR) هو سجل الكتروني للتجارب السريرية في لبنان. سيضم جميع التجارب التي تستهدف البشر ؛ مثل المجالات العلاجية التي تضم الأدوية ، والإجراءات الجراحية ، والتدابير الوقائية ، ونمط الحياة ، والأجهزة الطبية ، واستراتيجيات العلاج وإعادة التأهيل والعلاجات التكميلية.

دليل إستعمال السجل اللبناني للتجارب السريرية (LBCTR)

الموقع الإلكتروني للسجل اللبناني للتجارب السريرية (LBCTR)