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This introductory course provides learners with the necessary background required when working in a Good Clinical Practice (GCP) environment. Designed for those not directly interfacing with clinical research sites, the course includes application-based examples and the rationale behind GCP principles. Upon successful completion, a certificate is provided.
Course Learning Objectives- Describe the foundations, background, principles and application of ICH GCP
- Identify key regional regulations that impact the conduct of clinical trials
- Recognize the importance of complying with ICH GCP, as well as the impact of noncompliance
- Describe ICH GCP key roles and responsibilities in the conduct of clinical trials
Key Features Include: - High-level ICH GCP E6 R2 coverage
- Focus on practical application of GCP principles and application-based activities
- Glossary of terms, bookmarking tool, ongoing "knowledge checks" and post-course exam
- Includes a Barnett certificate of training
- Applicable for global clinical research professionals
Group Pricing Structure:
1-10 Users $199 per user
11-20 Users $179 per user
21-30 Users $169 per user
31-40 Users $159 per user
41+ Users $149 per user