ICH GCP : Good Clinical Practice (Free)
Comprehensive Modules for In Depth Knowledge (Read Only)
- Description
- Curriculum
- Reviews
What you learn? ICH GCP E6(R2) Requirements
- Pharmacy or Lifesciences background
Description
- This 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
What Benefits/ Value This Course Offer?
- Upgrade Yourself With New ICH GCP E6R2 Update
- Content Developed By Industry People With 15+ Years of Experience
- Self Paced Learning
Who this course is for:
- Clinical Research Organizations staff, students
ICH GCP ( Good Clinical Practice)
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1Introduction to Training Modules
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2Module 1: Introduction, Background and History of ICH GCP
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3Module 2: Glossary
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4Module 3 : Principles of ICH GCP
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5Module 4 : Roles and Responsibilities of IRB/IEC
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6Module 5 : Roles and Responsibilities of Sponsor
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7Module 6 : Roles and Responsibility of Investigator
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8Module 7 : Essential Documents
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