INNOVATIONS IN GLOBAL CLINICAL TRIALS Webinar Replay
ISO 14155:2020 GCP for Medical DevicesWEBINAR 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!
ISO 14155 2020 Safety and Adverse Events Video Lecture
ISO 14155:2020 GCP for Medical DevicesThis 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.

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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.
ISO 14155 2020 Overview Video Lecture
ISO 14155:2020 GCP for Medical DevicesTime: 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.

ISO 14155 2020 New Responsibilities of Sponsor/CRO Video Lecture
ISO 14155:2020 GCP for Medical DevicesLevel: Intermediate
Time: 20 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155: 2020 for sponsor and CRO responsibilities.

ISO 14155 2020 Responsibilities of Principal Investigator Video Lecture
ISO 14155:2020 GCP for Medical DevicesLevel: Intermediate
Time: 20 Minutes
This tutorial provides an accurate overview of the main changes introduced by ISO 14155:2020 for principal investigator responsibilities

ISO 14155 2020 Masterclass Video Course
ISO 14155:2020 GCP for Medical Devices
ISO 14155 2020 Ethical Considerations Video Lecture
ISO 14155:2020 GCP for Medical DevicesThis tutorial provides an accurate overview of the main changes introduced by ISO 14155: 2020 for Ethics and the informed consent process.

ISO 14155 2020 Clinical Trial From Start To Finish Video Lecture
ISO 14155:2020 GCP for Medical DevicesLevel: 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.
