Clinical Investigation of Medical Devices for Human Subjects Good Clinical Practice (ISO14155:2011)

Posted on:28 Oct 2015

Cystic Fibrosis Research Award

The course covers the GCP guidelines as outlined in the ISO 14155:2011 Standard for GCP in medical device studies. Participants also learn about basic ethical principles according to the Declaration of Helsinki and local regulations that apply. The lectures are augmented by workshops and discussion sessions. There is limited availability 20 places.

When & Where: This course will take place in Molecular Medicine Ireland ( on Monday 07th December from 10:00 to 16:00

Who should attend: The course is specifically designed for academics, early stage medical device companies and established companies who are planning to run clinical investigations with new innovative medical devices. Some of you have already attended this workshop so you may have a colleague or other company who this training may be of benefit.

Fees: Academia /SME rate – €100, Multinational/non-academic rate – €400

For registration:

For further details please see attached flyer here : CRCI GCP

Coronavirus (COVID-19)

In light of the Covid-19 situation, in advance of attending for a scheduled patient visit, please confirm the visit with your research nurse.