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Joint Research Management Office
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JRMO
Performing research
Conducting research with human participants (outside the NHS)
Frequently asked questions (FAQs)
In this section
Performing research
Responsible Research and Innovation
Conducting research in the NHS
Setting up a study
Running and closing a study
Other important issues
Conducting research with human participants (outside the NHS)
QMERC review routes for ethics approval
Block and International applications and Transfer of studies to Queen Mary
How to set-up a Devolved School Research Ethics Committee
How do I apply?
Post approval responsibilities
Risk considerations
Queen Mary Ethics of Research Committee and Meeting Dates
Breaches and complaints
Training
Documents guidance and resources
Frequently asked questions (FAQs)
Research Integrity
Allegations of Research Misconduct at Queen Mary
Authorship at Queen Mary
AI and research integrity
Avoiding predatory journals
Personal research access
Research facilities
Clinical facilities
Barts Health Clinical Research Facility
Royal London Hospital CRC
Whipps Cross Hospital CRU
Children's clinical research facility
Clinical Physics
HTRC
Role of the HTRC
The Human Tissue Act
Consent
HTRC training and contact
Lab services
Medical illustration
Pharmacy support
UK CRC Tissue Directory
Non-clinical facilities
Involving patients in research
PRES
PPI resources for researchers
Reimbursing expenses
PPI news
Seeking consent
Working with Patient Research Champions
Standard Operating Procedures (SOPs)
Guidance Documents
SOP 01
SOP 07a
SOP 07b
SOP 08
SOP 09
SOP 10
SOP 11a
SOP 11b
SOP 12a
SOP 12b
SOP 13a
SOP 13b
SOP 14
SOP 15
SOP 16a
SOP 16b
SOP 17a
SOP 17b
SOP 17c
SOP 18a
SOP 18b
SOP 19
SOP 20
SOP 21
SOP 22
SOP 23
SOP 24
SOP 25
SOP 26a
SOP 26b
SOP 26c
SOP 26d
SOP 27
SOP 28
SOP 29
SOP 31
SOP 33
SOP 34a
SOP 34b
SOP 38a
SOP 38b
SOP 38c
SOP 38d
SOP 39
SOP 40
SOP 41
SOP 42a
SOP 42b
SOP 43
SOP 45
SOP 46
SOP 47
Frequently asked questions (FAQs)
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