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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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Paediatric Consent: The practicalities and legalities in taking consent for paediatric trials
This course will be run jointly by Glasgow Clinical Research Facility and Edinburgh Clinical Research Facility.
This online workshop will focus on the ethical, legal and practical issues around obtaining informed consent for paediatric clinical research in Scotland. The first half of the course examines the legislation and guidance in relation to consent, with a specific focus on who is able to give consent, dependent on the type of trial and the age of the participant. The second section discusses how to implement the legislation by closely examining the consent process and highlighting practical considerations.
Suitable for all those involved in paediatric trials, the aim of the course is to provide participants with an improved knowledge of the subject and the confidence to apply best practice within their own work areas.
Please note: this course focuses on Scottish legislation.
Pricing Information:
NHS Invoice Detail:
Name NHS GREATER GLASGOW AND CLYDE Building CALEDONIA HOUSE Street CARDONALD BUSINESS CENTRE City GLASGOW Postcode G51 4ED Subject ENDOWMENT FUND CG0337 EDUCATION AND TRAINING Detail Please provide details of the training course, date and name of attendee on the purchase order and email copy to GG-UHBGlasgowCRFeducation@nhs.net.