| 1 x | ISO 14155 – Clinical Investigation Planning | € 236.00 |
| 1 x | European Safety Reporting Requirements during Clinical Investigations v3 | € 124.00 |
| 1 x | Deviations and Non-Compliance Handling | € 54.00 |
| 1 x | Importance of Clinical Investigator´s Brochure (IB) | € 332.00 |
| 1 x | Visit Report Writing | € 54.00 |
| 1 x | ISO 14155 version 2020 VS 2026 Gap Analysis | € 199.00 |
| 1 x | Good Documentation Practices for Clinical Study Files | € 161.00 |
| 1 x | Ethics Committee(EC) / Institutional Review Board Requirements | € 143.00 |
Ethics Committee(EC) / Institutional Review Board Requirements
Ethics Committee(EC) / Institutional Review Board Requirements
This course provides an overview of the basic Ethics Committee (EC) and Institutional Review Board (IRB) requirements according to 21 CFR 56, ISO 14155, and international law. It offers a practical approach to the EC and IRB processes and explains how to effectively manage the processes to prevent delays.
2 modules
€ 143.00
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