Local Training


GCP Courses

Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting studies that involve human participants. Attending GCP courses are an essential requirement for any researcher involved in commercial or non-commercial studies. Compliance with GCP provides assurance that the rights, safety and well-being of research subjects are protected and that the results of the study are credible.
 
Most courses are held in Room 115 (first floor) of the Health Sciences Building. A map will be sent alongside confirmation of course booking.

Online NIHR GCP (CTIMPs)

Who will benefit from this course?
Anyone conducting or supporting clinical trials involving CTIMPs  (Clinical Trial of Investigational Medicinal Products) . This option is also available for those who are required to revalidate their certificate and are unable to attend a face-to-face update.
 
How long will this course take?
It is recommended to allow 4 hours to complete this course however this can be different dependent on the individual delegate. 

Please email us at: 
nhsg.randdtraining@nhs.net for online registration details.
 

GCP CTIMPs (Update) - Med Chi Building

Who will benefit from this course?
Those who have previously completed a full GCP for Researchers (CTIMPs) course or an online GCP (CTIMPs) course who are looking to revalidate their certificate.
 
What will I learn?
Key topics include:
·        Responsibilities, Approvals Process & Trial Master Files
·        Pharmacovigilance
·        Quality Tools
·        MHRA Inspections
 
The next available course is on the 11th September 201412:45-16:00
Please email us at: nhsg.randdtraining@nhs.net to enquire about availability and receive a registration form. 
 

GCP for Researchers (Core) - Rm115, HSB

Who will benefit from this course?
Any researcher involved in studies that do not involve investigational medicinal products (IMPs). It is suitable for studies that are: observational; qualitative; using blood or tissue; analysing data from medical notes (and many more).
 
What will I learn?
This course will cover the principles of GCP through lecturing and interactive activities. Key topics include:
  • The Research Governance Framework
  • Informed Consent
  • Source Verification
  • Data Protection
  • Monitoring
 
Upcoming course dates are as follows:
 
 
 
 
 
Thursday 25th September 2014
 
13:00 - 16:00
 
Thursday 16th October 2014
  
 
14:00 - 17:00

Fiday 21st November 2014

13:00 - 16:00

Friday 12th December 2014

13:00 - 16:00

 
Please email us at: nhsg.randdtraining@nhs.net to enquire about availability and receive a registration form.
 

GCP for Researchers (Update) - Rm 115, HSB

Who will benefit from this course?
Any researcher involved in studies that do not involve investigational medicinal products (IMPs) who has previously completed a full GCP for Researchers course or an online GCP course which now requires revalidation.

 

What will I learn?

Key topics include:

    • The Principles of GCP
    • The Research Governance Framework
    • Recent and pending changes

 

 
 

 

Tuesday 9th September   

11:30 - 13:00                 FULL

Wednesday 10th  September 2014

09:30 - 11:00                 FULL

Wednesday 8th October 2014

10:00 - 11:30

Wednesday 5th November 2014

13:00 - 14:30

Tuesday 2nd December 2014

09:00 - 10:30

 

Please email us at: nhsg.randdtraining@nhs.net to enquire about availability and receive a registration form.

 

The Ethics Process - Rm 115, HSB

This course is for any researcher who has to apply for NHS ethics approval and finds the process challenging.
 
 

Wednesday 27th August 2014

CANCELLED

Wednesday 3rd September2014

10:00am - 12:30pm

Monday 29th September2014

10:00am - 12:30pm

Wednesday 29th October 2014

10:00am - 12:30pm

Wednesday 12th November 2014

10:00am - 12:30pm

Monday 8th December 2014

10:00am - 12:30pm

Please email us at: nhsg.randdtraining@nhs.net to enquire about availability and receive a registration form.

 

Research Practice Series Modules:

  • Informed Consent

Thursday 18th September 2014         13:00-14:00   FULL

Thursday 9th October 2014                09:00-10.30

Wednesda 5th November 2014          15:00-16:30

Wednesday 10th December 2014      09:00-10:30

     

  • Study Documentation

  • Thursday 28th August 2014                14:00- 16:00   FULL

    Friday 26th September 2014               14:00- 16:00   FULL

            

    •  

    • Online Modules

       

The MRC Regulatory Support Centre has developed the following modules:
  • Research Data and Confidentiality
  • Research and Human Tissue Legislation
  • IRAS