$199.00
From the EU Clinical Trials Directive to the Clinical Trials Regulation, the content includes an overview of the requirements for the conduct of clinical trials in the European Union, the EU Regulation and ICH E6(R2), ...
From the EU Clinical Trials Directive to the Clinical Trials Regulation, the content includes an overview of the requirements for the conduct of clinical trials in the European Union, the EU Regulation and ICH E6(R2), the EU Portal and Database (Clinical Trials Information System or CTIS), highlights of the EU Regulation 536/2014 (the Clinical Trials Regulation), and running clinical trials in the EU.
| Credit Hours | NA |
|---|---|
| Method of Training | Online, asynchronous, self-paced eLearning |
| Average Learning Time | 45 minutes |
| Enrollment Period | 12 months |
| Accessibility | 24/7 access to all program materials |
| Demonstration | Four (4) free trial courses are available |
| Group/Employee Training | Request a quote |
| Final Assessment | Multiple choice; unlimited attempts |
| Digital Badge | Issued upon completion |
| Certificate | Encrypted PDF with validation QR barcode |
