INNOVATIONS IN GLOBAL CLINICAL TRIALS
ISO 14155:2020 GCP for Medical DevicesDuration:  Unlimited
Cost:  99  USD
WEBINAR REPLAY
This webinar provides an overview of the innovations in clinical trials and provides practical suggestions on how to get ready now – as the standard is already effective and everyone is expected to comply!
Length: 00:30
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.
Length: 00:15
LEARN FOR FREE
RECORDED LIVE LECTURE - Dr. M. Tocchi
Time: 15 Minutes
This recorded video-lecture by Dr. Monica Tocchi, who contributed to the development of international standard ISO 14155 for clinical trials. This introductory course describes the key changes that affect pre-market studies and post-market trials for medical devices.
Length: 00:15
Version: 01
Release Date: 16 February 2020
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.
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.
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
Length: 00:20
Version: 01
Release Date: 1 April 2020
ISO 14155 2020 Masterclass
ISO 14155:2020 GCP for Medical DevicesDuration:  Unlimited
Cost:  495  USD
The ISO 14155 standard provides crucial guidance and support to any party involved in a clinical investigation - primarily to Sponsors (including monitors) and investigators, but also ethics committees, regulatory authorities and notified bodies implicated in the conformity assessment of medical devices.
Length: 02:00
Version: 01
Release Date: 20 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.
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.
Length: 00:35
Version: 01
Release Date: 30 March 2020