Video Lecture
Courses tagged with "Video Lecture"
Clinical Evaluation Upgrade to MDR
Clinical Evaluation 2020Duration: Unlimited
Cost: 79 USD
VIDEO LECTURE
Time: 39 minutes
Is your Clinical Evaluation ready for the MDR? Discover Meditrial e-learning and avoid delays for market access. Meditrial will guide you with easy steps. Learn at your own pace and reach your goals!
After the course, you can take a brief test to receive your certification. Enjoy!
Time: 39 minutes
Is your Clinical Evaluation ready for the MDR? Discover Meditrial e-learning and avoid delays for market access. Meditrial will guide you with easy steps. Learn at your own pace and reach your goals!
After the course, you can take a brief test to receive your certification. Enjoy!
Category: Clinical Evaluation 2020
Version: 01
Release Date: 17 February 2020
COVID-19 PPE Emergency
Covid-19Duration: Unlimited
Cost: 49 USD
Video Lecture
Time: 15 Minutes
The shortage of personal protective devices has endangered countless lives of healthcare operators working in COVID-19 treatment facilities. This is a widespread and prevalent issue worldwide.
After the course, you can take a brief test to receive your certification. Enjoy!
Category: Covid-19
LEARN FOR FREE
In the world today we need digital health. We will discuss what is the digital health revolution and in what way has Covid acted as the catalyzer. We will then get into what are the tools and technologies that are already out there today.
In the world today we need digital health. We will discuss what is the digital health revolution and in what way has Covid acted as the catalyzer. We will then get into what are the tools and technologies that are already out there today.
Category: Digital Health
Length: 00:20
INTERVIEW
LEARN FOR FREEThe Digital Health landscape is rapidly expanding and innovating. In this webinar Peter Fitzgerald delivers an informative and interesting presentation of digital health in the COVID Age and forward.
Category: Digital Health
Length: 00:20
LEARN FOR FREE
The Digital Health landscape is rapidly expanding and innovating. In this webinar Peter Fitzgerald delivers an informative and interesting presentation of digital health in the COVID Age and forward.
The Digital Health landscape is rapidly expanding and innovating. In this webinar Peter Fitzgerald delivers an informative and interesting presentation of digital health in the COVID Age and forward.
Category: Digital Health
Length: 00:30
Southern Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 Minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Level: All Levels
Time: 15 Minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Category: Europe Market Access
Version: 01
Release Date: 29 April 2020
Eastern Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Level: All Levels
Time: 15 minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Category: Europe Market Access
Version: 01
Release Date: 29 April 2020
Western Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Level: All Levels
Time: 15 minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Category: Europe Market Access
Version: 01
Release Date: 29 April 2020
Northern Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Level: All Levels
Time: 15 minutes
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
Category: Europe Market Access
Version: 01
Release Date: 29 April 2020
LEARN FOR FREE
What is GDPR?
When is it applicable?
Fines for Non-Compliance
GDPR and Clinical Trials
How to comply, practical approach
What is GDPR?
When is it applicable?
Fines for Non-Compliance
GDPR and Clinical Trials
How to comply, practical approach
Category: GDPR
Length: 00:10
Version: 01
Release Date: 18 April 2020
ISO 14155 2020 Safety and Adverse Events
ISO 14155:2020 GCP for Medical DevicesDuration: Unlimited
Cost: 99 USD
This lecture describes the key changes in the international ISO standard for clinical trials. In this module we will show you the main changes that have occurred compared to the ISO 14155 2011 in the safety and adverse event reporting.
Category: ISO 14155:2020 GCP for Medical Devices
Length: 00:15
ISO 14155 2020 Overview
ISO 14155:2020 GCP for Medical DevicesDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Time: 15 minutes
MDR is finally here and takes effect in May 2020! This video lecture provides you with an overview of the new regulations and clinical responsibilities set forth by the new ISO 14155 2020.
Time: 15 minutes
MDR is finally here and takes effect in May 2020! This video lecture provides you with an overview of the new regulations and clinical responsibilities set forth by the new ISO 14155 2020.
Category: ISO 14155:2020 GCP for Medical Devices
Length: 00:15
Version: 01
Release Date: 2 June 2020
ISO 14155 2020 New Responsibilities of Sponsor/CRO
ISO 14155:2020 GCP for Medical DevicesDuration: Unlimited
Cost: 99 USD
VIDEO LECTURE
Level: Intermediate
Time: 20 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155: 2020 for sponsor and CRO responsibilities.
Level: Intermediate
Time: 20 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155: 2020 for sponsor and CRO responsibilities.
Category: ISO 14155:2020 GCP for Medical Devices
Length: 00:20
Version: 01
Release Date: 20 April 2020
ISO 14155 2020 Responsibilities of Principal Investigator
ISO 14155:2020 GCP for Medical DevicesDuration: Unlimited
Cost: 99 USD
VIDEO LECTURE
Level: Intermediate
Time: 20 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155:2020 for principal investigator responsibilities
Level: Intermediate
Time: 20 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155:2020 for principal investigator responsibilities
Category: ISO 14155:2020 GCP for Medical Devices
Length: 00:20
Version: 01
Release Date: 1 April 2020
ISO 14155 2020 Ethical Considerations
ISO 14155:2020 GCP for Medical DevicesDuration: Unlimited
Cost: 99 USD
This tutorial provides an accurate overview of the main changes introduced by ISO 14155: 2020 for Ethics and the informed consent process.
Category: ISO 14155:2020 GCP for Medical Devices
Length: 00:20
Version: 01
Release Date: 12 April 2020
ISO 14155 2020 Clinical Trial From Start To Finish
ISO 14155:2020 GCP for Medical DevicesDuration: Unlimited
Cost: 99 USD
VIDEO LECTURE
Level: Intermediate
Time: 35 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155: 2020 for the Clinical Trial process. The clinical trial’s process is described from the beginning to the end: Planning, Conduct and Closeout.
Level: Intermediate
Time: 35 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155: 2020 for the Clinical Trial process. The clinical trial’s process is described from the beginning to the end: Planning, Conduct and Closeout.
Category: ISO 14155:2020 GCP for Medical Devices
Length: 00:35
Version: 01
Release Date: 30 March 2020
INTRODUCTION TO MEDICAL DEVICE REGULATION ROADMAP & ORIENTATION
New Medical Device Regulation (MDR)Duration: Unlimited
Cost: 49 USD
This course presents an overview of the new European regulation for medical devices and provides key information regarding new changes within the MDR. Learn all you need to know for a successful transition to the new legislative framework.
After the course, you can take a brief test to receive your certification. Enjoy!
Category: New Medical Device Regulation (MDR)