10
Mar

HRB CRCI Quality Working Group Establishment

HRB CRCI Quality Working Group Establishment. The HRB CRCI Quality Working Group (QWG) established a terms of reference for it’s operation on 3 March 2016. The group consists of quality and training representatives from each of the partner CRF/Cs and is chaired by the HRB CRCI Quality and Regulatory Affairs Manager, Ms. Sinead Curran. The mission of the QWG is

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9
Mar

HRB CRCI response to EMA consultation on the updated ICH E6(R2) on good clinical practice

HRB CRCI response to EMA consultation on the updated ICH E6(R2) on good clinical practice. The European Medicines Agency’s (EMA) recently consulted on the addendum to the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) E6 (R2) guideline on good clinical practice (GCP). The HRB CRCI QWG response can be found here: VIEW RESPONSE

19
Feb

Career opportunity with Molecular Medicine Ireland

Molecular Medicine Ireland in partnership with CÚRAM, the SFI Centre for Research in Medical Devices, seeks a high-calibre candidate to work in a collaborative centre of excellence on a well-resourced project that will develop key information and education tools for the medical devices research community. Please review the details of the role, responsibilities and person specification at the following link :

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16
Feb

HRB CRCI Website Launch

HRB CRCI is delighted to announce the launch of our new website. The goal of this website is to provide quick and easy access to information about HRB CRCI and it’s network that may be of interest to members of the public, healthcare professionals, life sciences industry and academia. The website outlines our services and activities and features information on the

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17
Nov

GCP Course Medical Devices 07 December 2015

MMI and CRCI have developed a GCP course specifically for Clinical Investigations in Medical devices. 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

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