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Research Quality & Standards Management

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Adverse Event/Incident Reporting Relating to Human Tissue for Research »17 June 2010

The purpose of this Standard Operating Procedure (SOP) is to describe the process of identifying, reporting and taking action on Adverse Events/ Incidents associated with the acquisition, storage,use and disposal of human tissues for research purposes. Approved by the Human Tissue Act Governance Group 17 June 2010.

Disposal of surplus and unusable human material »21 February 2011

The purpose of this Standard Operating Procedure (SOP) is to describe the disposal of all waste human relevant material (as defined by the Human Tissue Act 2004) pertaining to research purposes, Approved by the Human Tissue Act Governance Group 21 February 2011.

Governance Arrangements for the Administration of the Human Tissue Act at King's College London »17 June 2010

The purpose of this Standard Operating Procedure (SOP) is to describe the arrangements put in place to ensure appropriate governance of the Human Tissue Act Licence held by Kings College London. Approved by the Human Tissue Act Governance Group 17 June 2010.

Human Tissue Act - Standard Operating Procedure for the Creation, Retention and Destruction of Research Records »07 June 2012

The purpose of this Standard Operating Procedure (SOP) is to describe the creation and retention of research documents associated the collection of HTA relevant material. It also details the procedure for document destruction. Approved by the Human Tissue Act Governance Group 7 June 2012.

Human Tissue Act Compliance Audit for the Research Sector »17 June 2010

The purpose of this Standard Operating Procedure (SOP) is to describe the audit arrangements in place to monitor compliance with the Human Tissue Act. Approved by the Human Tissue Act Governance Group 17 June 2010.

Procedure for Investigating and Resolving Allegations of Research Misconduct »01 July 2009

The College's procedure for investigating allegations of misconduct by those carrying out research under the auspices of the College. Updated by Directorate of Research Management September 2012

Procedures for the Approval, Modification, Monitoring and Review of Programmes and Modules 2012-13 »10 October 2012

Procedures covering the approval, modification, monitoring and review of all programmes and modules. The procedures include a section on notes of guidance and web links to templates and forms. The word version form templates can be found on the Quality and Academic Support web pages (www.kcl.ac.uk/asq).

Production and Control of Standard Operating Procedures »17 June 2010

The purpose of this Standard Operating Procedure (SOP) is to describe the procedure to be followed to ensure that SOPs are produced in a consistent format and that they are adequately controlled so that staff work to the same closely controlled standards. Approved by the Human Tissue Act Governance Group 17 June 2010.

Seeking Consent for the Removal, Storage & Use of Relevant Material for Research Purposes »17 June 2010

The purpose of this Standard Operating Procedure (SOP) is to describe the procedure for providing information and seeking consent from participants of research studies where tissues or cells are to be procured (as defined by the Human Tissue Act 2004). Approved by the Human Tissue Act Governance Group 17 June 2010.

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