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CLINICAL RESEARCH AND THE NHS. Research and clinical governance Translational research using samples and data Qualitative research Multidisciplinary nature.

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Presentation on theme: "CLINICAL RESEARCH AND THE NHS. Research and clinical governance Translational research using samples and data Qualitative research Multidisciplinary nature."— Presentation transcript:

1 CLINICAL RESEARCH AND THE NHS

2 Research and clinical governance Translational research using samples and data Qualitative research Multidisciplinary nature of successful clinical research Considerations and regulatory approvals largely the same

3 Who do you need on board?  Clinician/surgeon  Statistician  Pathologist  Clinical Trialist  Research Nurse

4 What approvals are required before you start?  Ethical approval  R&D approval (NHS permission and site-specific)  Clinical trials: MHRA, GTAC  Sponsorship

5 Ethical approval: Where do you apply? Non-NHS participants University Ethics Review Committee With or without sample collection/storage? NHS staff, premises, facilities University Ethics Review Committee NHS patients National Research Ethics Service (NRES) All types of research with or without sample collection

6 Ethical review: What will be considered?  Identification and recruitment  Consent  Scientific validity of the study  Collection of samples; existing/prospective  Access to personal/clinical data; anonymisation  Storage and retention of personal data  Funding  Sponsorship  Incidental findings and feedback  What will happen to samples/data when study finished  Vulnerable groups

7 R&D approval: What will be considered?  Principal Investigator  Identification and recruitment  Consent  Location  Whether procedures are additional to clinical pathway  Access to personal/clinical data; anonymisation  Storage and retention of personal data  Sponsorship  MONEY!

8 Clinical trials  Clinical trial authorisation from the MHRA  GTAC  Good Clinical Practice  Contractual agreements  Quality Management System  Adverse event reporting

9 Sponsor Under the Research Governance Framework …… Requirement for all research using NHS patients, staff and facilities The Sponsor is legally responsible for the management of the research  Investigators appropriate  Funding  Regulatory approvals  Insurance  Current legislation e.g. Human Tissue Act, DPA

10 Integrated Research Application Service (IRAS) Streamlining the research application process https://www.myresearchproject.org.uk/  Ethical approval  NHS permission/R & D approval  MHRA  GTAC  NOMS, MOJ


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