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تدريب صيفي - وظائف
انشاء حساب / دخول
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تدريب صيفي
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دورات تدريبية
Science
Clinical Research Essentials: ICH GCP & Study Designs Series
محتوى الدورة
11th Series - History Pharmacovigilance
Pharmacovigilance methods #ytshorts
Establishment Pharmacovigilance Centre #ytshorts
19th Series - Pharmacoeconomics - Part B
18th Series - Pharmacoeconomics - Part A
17th Series - Pharmacoepidemiology
16th Series - Pharmacovigilance Softwares
15th Series - National International Pharmacovigilance Scenario - Statistical methods
14th Series - Passive Surveillance Active Surveillance Vaccine Safety Surveillance
13th Series - WHO International Drug Monitoring Program & Pharmacovigilance Program of India
12th Series - International Classification of Diseases & International Nonproprietary Names of Drugs
1st Series - ICH GCP Guidelines for Clinical research
10th Series - ADR Spontaneous reporting Predictability and Preventability assessment of ADRs
9th Series - Terminologies - Detection and Reporting of ADRs
8th Series - Adverse Drug Reactions ADR
7th Series - Clinical trial documentation
6th Series - Clinical trial personnel - Roles and responsibilities
5th Series - Cross Sectional study
4th Series - Non-randomized Control Trial and Observational studies
3rd Series - Institutional Review Board and Randomized Control Trial
2nd Series - Informed consent
للحصول على شهادة
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التسجيل
2- مشاهدة الكورس كاملا
3- متابعة نسبة اكتمال الكورس تدريجيا
4- بعد الانتهاء تظهر الشهادة في الملف الشخصي الخاص بك
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