Research & Development Directorate

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Carrying out Research > SOP Library

The following SOPs are designed for use in research being carried out within the Trust.

No. Title Version Last update
       
Index of Standard Operating Procedures v.1.0 July 2008
2 Adverse event management v.2.4 April 2008
2a Annual Safety Reporting v.1.1 April 2008
3 Allocation of sponsorship v.1.0 April 2008
4 Delegation of responsibilities v.1.1 April 2008
5 GCP inspection procedure (MHRA) v.1.0 April 2008
7 Incident reporting v.1.0 April 2008
8 Project Registration and Approval v.1.2. April 2008
9 Project suspension v.1.0 April 2008
10 Routine random active project audit v.2.2 April 2008
10a For-cause project audit v.1.0 April 2008
10b Human Tissue Audits v.1.0 April 2008
11 Document storage v.2.1 April 2008
12 Informed consent v.2.0 April 2008
13 Human Tissue Act compliance v.1.0 April 2008
13a Anonymisation of tissue samples v.1.0 April 2008
13b Using tissue from a tissue bank v.1.0 April 2008
13c Sample numbering v.1.0 April 2008
13d Sample logging, storage and tracking v.2.0 April 2008
13e R&D management of tissue studies v.1.0 April 2008
13f Import and export of tissue v.2.0 April 2008
14 Sponsor Files v.1.0 April 2008
15 Writing a protocol v.1.0 April 2008
16 CTA Applications v.2.0 April 2008
17 Making Amendments v.1.0 April 2008
18 Urgent Safety Measures v.1.0 April 2008
19 Considerations for Potential Pregnancy v.1.0 April 2008
20 Sponsoring a Clinical Trial of Investigational Medicinal Product v.1.0 April 2008
20a Post Trial Treatment Responsibilities v.1.0 May 2008
21 Non Investigational Medical Products - NIMPS v.1.0 April 2008
22 Genetic Modification Experiments Categorised at Levels 1 and 2 v.1.0 April 2008
22a Receipt of Class 1 Gene Therapy Products.doc v.1.0 June 2008
22b Storage of Class 1 Gene Therapy Products v.1.0 June 2008
22c Transportation of Class 1 Gene Therapy Products v.1.0 June 2008
22f Accidental Inoculation and Blood Spillage in Genetherapy v.1.0 July 2008

 
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