Table of Forthcoming Courses


Date Course Time Venue
11/08/10 GCP Update 9.30am - 1pm Tutorial Room,
Tennent Building, Western Infirmary
30/08/10 SOP Workshop 9.30am - 1pm Conference Room,
Tennent Building, Western Infirmary
02/09/10 GCP Update 9.30am - 1pm Tutorial Room,
Tennent Building, Western Infirmary
23/09/10 GCP Full Day Tennent Building, Western Infirmary
22/09/10 GCP Update Tennent Building, Western Infirmary
07/10/10 Research for GCP
(Non Drug Trials)
9.30am - 1pm Conference Room,
Gardner Institute, Western Infirmary
(Please note change of date and venue)
11/10/10 Pharmacovigilance 9.30am - 10.30am Conference Room,
Tennent Building, Western Infirmary
14/10/10 GCP Full Day Lecture Theatre,
Tennent Building, Western Infirmary
(Please note change of venue)
04/11/10 Research for GCP
(Non Drug Trials)
9.30am - 1pm Lecture Theatre,
Tennent Building, Western Infirmary
22/11/10 GCP Full Day Tennent Building, Western Infirmary
(Please note change of venue)
24/11/10 GCP Update
Beatson Gartnavel Hospital
06/12/10 Pharmacovigilance

9.30am - 10.30am Conference Room,
Tennent Building, Western Infirmary
09/12/10 GCP Update Tennent Building, Western Infirmary
15/12/10 SOP Workshop

9.30am - 1pm Conference Room,

Tennent Building, Western Infirmary
20/12/10 GCP Full Day Tennent Building, Western Infirmary
03/03/11 Research for GCP
(Non Drug Trials)
9.30am - 1pm Lecture Theatre, Tennent Building, Western Infirmary
16/03/11 SOP Workshop 9.30am - 1pm Conference Room,
Tennent Building, Western Infirmary

Introduction to Good Clinical Practice - Full Day

The course is appropriate for those who are conducting or supporting Clinical Trials of an Investigational Medicinal Product (CTIMP) and, as such, are required to provide evidence of GCP training.

This course is relevant to individuals who have no previous GCP training and those whose previous GCP training was more than two years ago.

Topics include:

  • History of clinical trials and the development of GCP.
  • Informed consent
  • Responsibilities of research personnel
  • Principles of GCP
  • Pharmacovigilance
  • Monitoring

Policy for Good Clinical Practice Training

Register for the GCP Course Full Day
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Confirmation will be sent on receipt of your application, this will secure your place on preferred date.

You will receive a detailed pack prior to the course. If you have not received this 7 days prior to date, please contact us at the email address below. sandrakane@nhs.net

PAYMENT

The course is free to all NHS and University staff.
External Applicants - Full Day fee £150.
Payment by cheque made payable to: NHSGG&C Endowment Fund (724110)

Update on Good Clinical Practice-Half Day

This course is relevant for those who are conducting or supporting Clinical Trials of an Investigational Medicinal Products (CTIMP) and who have previously undertaken a GCP course and wish to update or re-fresh their knowledge.

It is particularly suitable for those who are conducting or supporting CTIMP and, as such, are required to provide evidence of having maintained and updated their knowledge of GCP.

Attendance at the half day update course requires you to have undertaken GCP training within the past two years.

Topics include:

  • Principles of GCP
  • MHRA inspections
  • Pharmacovigilance
  • Quality Tools
  • Trial master files
  • Responsibilities in research team

Policy for Good Clinical Practice Training

Register for the Update on Good Clinical Practice - Half Day
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Confirmation will be sent on receipt of your application, this will secure your place on preferred date.

You will receive a detailed pack prior to the course. If you have not received this 7 days prior to date, please contact us at the email address below. sandrakane@nhs.net

PAYMENT

The course is free to all NHS and University staff.
External Applicants - Half Day fee £75
Payment by cheque made payable to: NHSGG&C Endowment Fund (724110)

Pharmacovigilance for CTIMP's

This workshop is intended for research personnel involved in clinical trials of investigational medicinal products (CTIMPs) sponsored by NHSGGC.

It is particularly relevant to those who are responsible for recording, assessing, or reporting drug related safety issues.

AIM

The aim of the workshop is to equip attendees with the knowledge and skills they require to fulfil their responsibilities in safety reporting.

OBJECTIVES

On completion of the workshop attendees will:

  • Define the terms used in Pharmacovigilance
  • Know who is responsible for safety reporting
  • Identify and assess medical events for seriousness, causality and expectedness
  • Apply the process for safety reporting in CTIMPs sponsored by NHS GGC
Register for the Pharmacovigilance Course
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Confirmation will be sent on receipt of your application, this will secure your place on preferred date.

You will receive a detailed pack prior to the course. If you have not received this 7 days prior to date, please contact us at the email address below. sandrakane@nhs.net

Recipes for Success - Standard Operating Procedure (SOP) Writing Workshop

This half day course, which mixes short lectures with practical activities, is appropriate for those involved in clinical research in any context, and who will be required to write and/or manage SOPs.

Topics include:

  • Understanding the importance of SOPs
  • Knowing how to write an SOP
  • Knowing how to manage an SOP
This session is relevant for individuals who have no previous SOP writing experience and for those who wish to improve their skills.
Register for the SOP Workshop
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Confirmation will be sent on receipt of your application, this will secure your place on preferred date.

You will receive a detailed pack prior to the course. If you have not received this 7 days prior to date, please contact us at the email address below. sandrakane@nhs.net

PAYMENT

Fee £35
Payment by cheque made payable to: NHSGG&C Endowment Fund (724110)

Good Clinical Practice for Research (Non-drug Trials)

This half-day course is appropriate for anyone conducting or supporting clinical research that does not involve a 'drug'.

The course will provide research staff with the knowledge to undertake quality research in accordance with the Research Governance Framework, which requires the application of the principles of Good Clinical Practice to all health research involving patients.

Topics include:

  • History of the Research Governance Framework
  • Informed Consent
  • Roles & Responsibilities
  • Quality Issues
  • Principles of GCP
Register for the Research for GCP (Non Drug Trials)
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[?]
[?]
[?]
[?]
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Confirmation will be sent on receipt of your application, this will secure your place on preferred date.

You will receive a detailed pack prior to the course. If you have not received this 7 days prior to date, please contact us at the email address below. sandrakane@nhs.net

PAYMENT

Fee £35
Payment by cheque made payable to: NHSGG&C Endowment Fund (724110)

Training Session

Current Courses

Table of Forthcoming Courses

Click on the course you are interested in below to see full details and register online

Introduction to Good Clinical Practice - Full day

Update on Good Clinical Practice - Half Day

Pharmacovigilance

Recipes for Success - Standard Operating Procedure (SOP) Writing Workshop

Good Clinical Practice for Research (Non-drug Trials)

We also offer courses in other areas of Scotland - Register for these through
Clinical Research Training for Scotland

IRAS Online Training Module

An online module has been added to the IRAS website to guide new users through IRAS. The module, which is free, explains how IRAS is structured and guides users through how to prepare and make applications using IRAS.

IRAS Website