H01 Patient Information Sheet Online Workshop Making Patient Info Sheets Clear & AccessibleInfo Location Attendee Categories Contact More Info Event Information![]()
DescriptionPatient Information Sheets (PIS) are a key document for potential participants to make an informed decision about whether to take part in a clinical study. While there is clear guidance from the Health Research Authority (HRA) on content and regulatory requirements, PIS are customised for each clinical trial and the specific patient population. Choosing the right language and format for patient facing materials for research studies and clinical trials still greatly varies and depends on the skills and experience of the team putting them together.
In this workshop attendees will gain valuable insights how to improve the format, language and delivery of the PIS working with clinical trial professionals and, patient and public representatives.
The workshop includes: an overview of the HRA guidance on the PIS design, an introduction to writing in plain English and accessibility a patient perspective group work in breakout rooms with trial professionals and patient and public representatives to review a draft PIS
Preparation: Review a draft PIS before the workshop (up to 1 hour preparation time).
After the course, attendees will receive a “PIS Checklist”: a summary of top tips when designing a Patient Information Sheet.
Event Location![]()
Attendee Categories3) Attendees From For-Profit Organisations.
Additional ItemsContactFor all queries relating to this Course please contact the following :- Daisy Kirkwood
PLEASE ONLY CONTACT THE ONLINE STORE DIRECTLY IF YOU ARE EXPERIENCING PROBLEMS WITH YOUR DEBIT/CREDIT CARD PAYMENT, FOR ALL OTHER QUERIES RELATING TO THIS COURSE, INCLUDING CANCELLATIONS THESE SHOULD BE DIRECTED TO THE CONTACT DETAILS ABOVE. More InformationCourse tutors:
Fees are based on the attendee's organisation as follows:
£0 free for attendees from units within the Institute of Clinical Trials and Methodology (ICTM) which are: • Cancer Research UK & UCL Cancer Trials Centre • Comprehensive Clinical Trials Unit at UCL • Medical Research Council Clinical Trials Unit at UCL • PRIMENT Clinical Trials Unit
The free places require a password to book, if you work within the ICTM please email ctc.training@ucl.ac.uk to request this. Emails must be sent from your UCL account and include your name, job title, and the department which you are working in. A cancellation fee of £50 will be charged to your department for late cancellations (less than 14 days) and no-shows for all courses.
Other UCL attendees who are required to pay the course fee can do this by reserving a free place on the online store and then paying by IDT, please email ctc.training@ucl.ac.uk who can assist you with this.
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