| 1 x | Clinical Evaluation Report: Review for Regulatory Professionals | € 308.00 |
| 1 x | GCP for Investigators: Ethics and Legal Processes for Medical Device Clinical Investigations | € 84.00 |
| 1 x | ISO 14155_课程1_范围 | € 143.00 |
| 1 x | test training for stg env | € 12.00 |
| 1 x | second video test | € 9.00 |
| 1 x | 临床试验的启动 | € 95.00 |
| 1 x | 临床试验关闭或终止 | € 66.00 |
| 1 x | US Safety Reporting Requirements during Pre-Market Clinical Trials | € 72.00 |
| 1 x | Duplicate of wmdos-34 | € 20.00 |
| 1 x | GCP for Investigators: Clinical Investigation Close out or Termination | € 66.00 |
| 1 x | Clinical Evaluation for Market Approval | € 616.00 |
| 1 x | GCP for Investigators: How to Qualify for Medical Device Clinical Investigations | € 95.00 |
| 1 x | GCP for Investigators: Introduction to Medical Devices | € 126.00 |
| 1 x | Managing Data Release Consent During Post Market Studies | € 75.00 |
| 1 x | European Safety Reporting Requirements during Clinical Investigations | € 90.00 |
| 1 x | Medical Device GCP for Investigators | € 120.00 |
| 1 x | Understanding Clinical Evaluation for Notified Body and Regulatory Professionals | € 544.00 |
| 1 x | GCP for Investigators: Initiation of a Medical Device Clinical Investigation | € 95.00 |
| 1 x | ISO 14155_课程3_临床试验策划 | € 180.00 |
| 1 x | ISO 14155_课程4_临床试验的开展 | € 143.00 |
| 1 x | Medical Device GCP – Investigator Certificate | € 255.00 |
| 1 x | ISO 14155_课程5_临床试验关闭 | € 90.00 |
| 1 x | Importance of Clinical Investigator´s Brochure (IB) | € 332.00 |
Medical Device GCP – Investigator Certificate
Medical Device GCP – Investigator Certificate
This program provides investigators and clinical investigation site personnel with a comprehensive introduction to the medical device regulatory environment. It offers an in-depth look at the criteria every investigator should consider before deciding to participate in a medical device clinical investigation.
It covers the following topics:
- Ethical and legal requirements of medical device clinical investigations
- How to ensure a successful investigation initiation
- Effective collaboration with sponsors during investigations
- Requirements for closing down clinical investigations
The content of this program is based on:
- ISO 14155: 2020 - Clinical Investigation of Medical Devices for Human Subjects
- The Declaration of Helsinki
- 21 CFR 812: Investigational Device Exemption
- 21 CFR 50: Protection of Human Subjects
ID: N43
213 minutes
6 trainings
€ 255.00
Add to Cart
| Course | ID | Duration | |
|---|---|---|---|
GCP for Investigators: Introduction to Medical Devices |
193 | 52 minutes | |
GCP for Investigators: How to Qualify for Medical Device Clinical Investigations |
200 | 32 minutes | |
GCP for Investigators: Ethics and Legal Processes for Medical Device Clinical Investigations |
212 | 25 minutes | |
GCP for Investigators: Initiation of a Medical Device Clinical Investigation |
202 | 30 minutes | |
GCP for Investigators: Clinical Investigation Conduct and Reporting |
204 | 51 minutes | |
GCP for Investigators: Clinical Investigation Close out or Termination |
206 | 23 minutes |
Learning Objectives
Upon successfully completing this program, learners will be able to:
- Understand the basic medical device regulatory principles for conducting clinical investigations
- Pay special attention to the risk management profiles of investigational devices, which will enable sound decisions prior to and during clinical investigations and ensure patient safety
Who Should Enroll
Clinical Investigator, and Clinical Study Coordinator.
Prerequisite Knowledge
No pre-requisites are required for this course.