Research & Development Directorate

Link to Trust website

Carrying out Research > SOP Library

The following Code Of Practices (COPs) are designed for use in research being carried out within the Trust.

               
      Title   Version   Last update
               
            Genetic Modification Experiments Categorised at Level 1  1.0  February 2009
               
               

The following Standard Operating Procedures (SOPs) are designed for use in research being carried out within the Trust.

               
  SOP No.   Title   Version   Last update
               
     1  Standard Operating Procedure for SOPs.doc  1.1  June 2009
     2  Adverse Event Management  2.5  June 2009
     2a  Annual Safety Reporting  1.2  June 2009
     3  Allocation of Sponsorship  1.1  June 2009
     4  Delegation of Responsibilities  1.1  April 2008
     5  GCP Inspection Procedure (MHRA)  1.0  April 2008
     7  Incident Reporting  2.0  June 2009
     8  Project Registration and Approval  1.2  April 2008
     9  Project Suspension  1.0  April 2008
     10  Routine Random Active Project Audit  2.4  June 2009
     10a  For-Cause Project Audit  1.2  June 2009
     10b  Human Tissue Audits  1.2  June 2009
     11  Document Storage  2.1  June 2009
     12  Informed Consent  2.1  June 2009
     13  Human Tissue Act Compliance  1.1  June 2009
     13a  Anonymisation of Tissue Samples  1.1  June 2009
     13b  Using Tissue from a Tissue Bank  1.0  April 2008
     13c  Sample Numbering  1.1  June 2009
     13d  Sample logging, Storage and Tracking  1.1  June 2009
     13e  R&D management of Tissue Studies  1.0  April 2008
     13f  Import and Export of Tissue  2.0  April 2008
     15  Writing a Protocol  1.0  April 2008
     16  CTA Applications  2.1  June 2009
     17  Making Amendments  1.2  June 2009
     18  Urgent Safety Measures  1.1  June 2009
     19  Considerations for Potential Pregnancy  1.0  April 2008
     20  Sponsoring a Clinical Trial of Investigational Medicinal Product  1.0  April 2008
     20a  Post Trial Treatment Responsibilities  1.0  May 2008
     21  Non Investigational Medical Products - NIMPS  1.0  April 2008
     22  Genetic Modification Experiments Categorised at Levels 1 and 2  1.0  April 2008
     22a  Receipt of Class 1 Gene Therapy Products  1.0  June 2008
     22b  Storage of Class 1 Gene Therapy Products  1.0  June 2008
     22c  Transportation of Class 1 Gene Therapy Products  1.0  June 2008
     22d  Containment and Room Facility of Class 1 Gene Therapy Products  1.0  May 2008
     22e  Waste Disposal of Class 1 Gene Therapy Products  1.0  May 2008

 
| Site Map | Contact Us | © 2009 University Hospital of South Manchester NHS Foundation Trust