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CANRISK -GP
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NOAR
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Training
Good Clinical Practice
API Scheme & PI Essentials
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CREATE Training
Informed Consent Training
Introduction To Clinical Research In The NHS Training
EDGE
Join Dementia Research
Resources
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Promoting Research
RCGP Research Ready
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GENOMICS
Studies
Industry Studies
News and Events
Newsletters
PRIDES
ABC-DS
BEACON
CANRISK -GP
COPD & Assistive Technology
ESCAPE - RCT STUDY
INJECTABLE MEDICATION (JAms)
NOAR
OPACE
PHILM GP 59959
RELIEF
SPIROMAC
The ELSA Study
Our Team
SOPs and WIs
Standard Operating Procedures (SOPs)
SOP 01 - Informed consent V.8
SOP 02 - Document management V.4
SOP 03 - Study set up V.6
SOP 04 - Study conduct approval V.
7
SOP 05 - Safety reporting V.5
SOP 06 - Management of SOPs and WIs V.6
Working Instructions (WIs)
WI 01 - Informed Consent - Minors V.4
WI 02 - Informed Consent - Adults Lacking Capacity V.6
WI 04 - Telephone Contact V.8
WI 05 - Site Identification for NIHR Industry Studies V.5
WI 06 - Opportunistic Recruitment V.5
WI 07 - Feasibility and Do-ability Assessments V.5
WI 08 - Initiation Visit V.7
WI 09 - GCP and Training Records V.8
WI 10 - Study Files and Filing V.6
WI 12 - Data Protection V.7
WI 13 - CRF Completion V.6
WI 16 - Audit and Inspection V.6
WI 17 - Monitoring Visit V.5
WI 18 - Archiving and Destroying Documents V.6
WI 19 - Study Close Down V.6
WI 20 - Adverse Event Reporting V.6
WI 21 - Serious Adverse Event Reporting V.6
WI 22 - Informed Consent of Adults With Communication Difficulties V.6
WI 23 - Informed Consent - Competent Adults V.5
CRN Glossary of Terms and Abbreviations
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