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ICH GCP : Good Clinical Practice (Audio + Test +Certificate)
Comprehensive Modules for In Depth Knowledge (with case studies and explanation)
- Description
- Curriculum
- Reviews
What you’ll learn
- Good Clinical Practice as given in E6(R2) Guideline by ICH
Requirements
- Pharmacy or Lifesciences background
Description
- This ICH GCP : Good Clinical Practice course gives an opportunity to get in depth knowledge of ICH GCP.
Who Should Enroll?
- Any Life Science/ Pharmacy/ Nursing/ Medical/ Dental Graduate or Post Graduate
Industry People:
Clinical Research Coordinator, Clinical Research Associate, Clinical Data Coordinator, Drug Regulatory Affairs Executive, Ethics Committee Members, Clinical Site Personnel, Any Professional Involved directly or indirectly in Clinical Research Activities
What This Course Covers?
- Module 1 Introduction purpose history of ICH GCP
- Module 2 Glossary Core Principles
- Module 3 13 core principles
- Module 4 Roles and responsibilities – IEC
- Module 5 Roles and responsibilities – Sponsor
- Module 6 Roles and responsibilities – Investigator
- Module 7 Essential documents
- Module 8 Case studies
What Benefits/ Value This Course Offer?
- Upgrade Yourself With New ICH GCP E6(R2) Update
- Content Developed By Industry People With 15+ Years of Experience
- Self Paced Learning with full explanation narrated for each module
- Practice questions in all modules and a final assessment quiz
Who this course is for:
- Clinical Research Organizations staff, students
Introduction Glossary, Principles of ICH GCP
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1IntroductionPreview Video lesson
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2Module 1: Introduction, Background and History of ICH GCP06:14
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3Practice test for Module 1: Introduction, Background & History of ICH GCP3 questions
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4Module 2: Glossary15:50
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5Practice quiz: Module 2: Glossary5 questions
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6Module 3: Principles of ICH GCP04:04
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7Practice quiz: Module 3 : Principles of ICH GCP4 questions
Roles and Responsibilities and Essential Documents
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8Module 4 : Roles and Responsibilities of IRB/IEC07:00
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9Practice quiz: Module 4: Roles and Responsibilities of IRB/IEC4 questions
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10Module 5: Roles and Responsibilities of Sponsor11:37
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11Practice quiz: Module 5 : Roles and Responsibilities of Sponsor4 questions
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12Module 6: Roles and Responsibility of Investigator07:56
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13Practice quiz: Module 6 : Roles and Responsibility of Investigator4 questions
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14Module 7 : Essential Documents7.35
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15Practice quiz: Module 7 : Essential Documents2 questions
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16Module 8 : Case Studies and Hypothetical Scenarios10:57
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17Practice quiz: Module 8 : Case Studies and Hypothetical Scenarios4 questions
End of Course Assessment
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Course details
Duration
2:45 hours
Lectures
9
Video
2:45 hours
Quizzes
9
Level
Advanced
Basic info
This course includes:
- 1.5 hours on-demand video
- 2 practice tests
- Access on mobile and TV
- Full lifetime access
- Certificate of completion
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