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- NRS Introduction to Good Clinical Practice (GCP)
- NRS Good Clinical Practice (GCP) Update
- Principal Investigator Roles and Responsibilities Workshop
- Bite Size Training - Investigational Medicinal Products
- Bite Size Training - Quality and Monitoring in Research Trials
- Bite Size Training - Getting started in a research trial
- Bite Size Training - Delivering a Research Trial
- Bite Size Training - The who's who of research and innovation
- Bite Size Training - Trial Design
- CTIMP Workshop
- Early Phase Clinical Trial
- Good Research Practice (Non-drug Trials)
- Informed Consent - Adults: Ethical, legal and practical aspects in clinical research
- Induction One: Clinical Research 101: Diving into research essentials
- Induction Two: Safe and Sound: Ensuring excellent research evidence
- Induction Three: In Pursuit of Perfection: Delivering quality research
- Laboratory Skills Workshop
- Medical Device Good Research Practice
- Paediatric Consent: The practicalities and legalities in taking consent for paediatric trials
- Preparing Poster and Presentations
- Introduction to Critical Appraisal
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The Education team works closely with our partners in the NHS, Higher Education Institutes and Research & Development departments to provide a service that is tailored to meet the needs of researchers and associated staff.
We collaborate with education staff in CRF's across the UK and with colleagues at the NIHR to ensure a cohesive and standardised programme of educational opportunities are available to researchers.
If you have any questions regarding the education programme or a course you have booked, please contact ggc.glasgowcrfeducation@nhs.scot or 0141 314 0206.
Glasgow Clinical Research Facility privacy statement
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CTIMP Workshop
The aim of this workshop is to equip clinical research staff with an understanding of the key elements involved in conducting a clinical trial of an investigational medicinal product (CTIMP). The course builds on GCP knowledge and assumes GCP training has been completed prior to attendance.
The workshop will consist of a mixture of presentations, case studies and practical exercises. It is relevant to those who are new to research and for those who would like to improve their understanding of clinical trials involving an investigational medicinal product
After the Workshop, each Participant will:
- Understand relevant CTIMP terminology and the requirements for CTIMPs including permissions and approvals
- Demonstrate the use of a protocol in setting up a CTIMP and planning a study visit
- Describe the key issues that impact on recruitment and retention
- Describe the key elements relating to the management of the investigational medicinal product (IMP)
- Recognise the importance of accurate documentation throughout all trial-related activities
- Understand the importance of safety measures and parameters in CTIMPs and the responsibilities of the research team in monitoring these
Pricing Information:
NHS Greater Glasgow and Clyde, NHS Lanarkshire, NHS Dumfries and Galloway, NHS Waiting Times Centre, NHS Ayrshire and Arran Free Other NHS £80 University £120 Commercial Organisation £290 Invoice Detail:
Name NHS GREATER GLASGOW AND CLYDE Building CALEDONIA HOUSE Street CARDONALD BUSINESS PARK City GLASGOW Postcode G51 4ED Subject ENDOWMENT FUND CG0337 EDUCATION AND TRAINING Detail To pay for courses please send a purchase order number along with name and date of course, name of attendee and email to ggc.glasgowcrfeducation@nhs.scot Please note confirmation of course will be sent once a purchase order number has been provided.
Pay by Card
Please contact our Treasury Department with the name of course and course date - 0141 278 2794
Please check back for new dates and locations being announced