Skip to content
Skip to navigation menu

 

Training

Good Clinical Practice (GCP) Training

The GCP policy is available to view/download via the link below.

 

GCP training policy
GCP Policy [123.9 Kb]

 

All researchers involved in a Clinical Trial of an Investigational Medicinal Product (CTIMP), i.e. a study which falls under the Medicines for Human Use (Clinical Trials) Regulations 2004, are legally obliged to conduct their research study in compliance with Good Clinical Practice (GCP).

It is a requirement that all members of a trial team identified on the Trial Delegation Log, not just the Chief Investigator/ Principal Investigator (CI)/ (PI), complete GCP training. GCP training should be renewed every two years.

NISCHR CRC is one organisation that provides courses on GCP training. Please click here for a list of NISCHR CRC training opportunities and dates.

GCP training is also available from other providers. When available, dates will be displayed below.

Latest GCP Training News:
Half-day GCP Training Course- 'Introduction to Good Clinical Practice' 29th March 2012.

Cardiff and Vale UHB will be hosting a half-day GCP training seminar which is open to all those involved in Clinical Trials who require Good Clinical Practice and EU Clinical Trials Directive training. The course will be run by The Institute of Clinical Research and will take place on Thursday 29th March, 09:00-12:45 pm in Lecture Theatre 3, Upper Ground Floor A Block, UHW, Heath Park Campus, Cardiff.

This course is useful both as a refresher for more experienced staff, and as an introduction for those who are completely new to clinical trials. Details of the course can be found  here .

The course is free of charge but places are limited and booking is mandatory. Please book your place using this form .

For any queries and to make your booking, please email: Research.Governance@wales.nhs.uk

GCP Training Seminars - A joint Cardiff University and Cardiff & Vale UHB Training Programme

A new GCP training scheme has been developed by Cardiff University and Cardiff and Vale UHB. The programme consists of a series of GCP related seminars which will count towards update GCP training for researchers. The 2011-12 programme can be found here.  

To book a place on any of these training seminars please contact Ross Bowden: ross.bowden@wales.nhs.uk

GCP Training Seminars 2011-12 Presentation Slides

 

Clinical Trials Regulation [1.4 Mb]

Clinical Trials Regulation - Presentation by Zoe Whale


Data Management [1.7 Mb]

Data Management - Presentation by SEWTU


Data Protection and Confidentiality [1.4 Mb]

Data Protection and Confidentiality - Presentation by Nic Drew


Essential Documentation [208.0 Kb]

Essential Documentation - Presentation by Anne Thomas


IMP Management [1.7 Mb]

IMP Management - Presentation by Angela Hallam


IMP Management At Site [1.5 Mb]

IMP Management At Site - Presentation by Kathryn Bethune


Online training

Online GCP training can be found at the following websites:

http://www.gcptraining.org.uk

http://www.ukcrn.org.uk/index/training/courses.html 

Research Governance Training Presentations

Click on the links below to view the slides from Research Governance presentations given by the Research Governance Team:

IRAS (Integrated Research Application System) Training  

The last IRAS Training session was held on 28/09/11. Please check this page regularly for information on future IRAS training events.

NISCHR Permissions Coordinating Process Presentations

The NISCHR Permissions Coordinating Unit will be launched from 4th July 2011 to coordinate the process of gaining NHS research permissions across Wales. For further information please contact: Ruth Baxter, NISCHR Permissions Co-ordinating Unit (PCU);
E-mail:  Ruth.baxter@wales.nhs.uk Tel: 01874 712540