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TASC Policies

 

Policy 

Title

 1.0_v3.0
Drug Accountability in Clinical Trials of Investigational Medicinal Products
 2.0_V3.0
Pharmacovigilance and Safety Reporting
 3.0_V5.0
Clinical Research Quality Management System
 4.0_V3.0
GCP Monitoring policy
 5.0_V3.0
Good clinical practice training policy for personnel involved in clinical research  
 6.0_V4.0
TASC publication policy: guidance for trialists
 7.0_V2.0
Negotiation and Signatures of Agreements of Investigator-led Clinical Trials Sponsored by University and/or the Board
 8.0_V2.0
Commercial Research Services
NHS Tayside Policies 
The NHS Tayside policies for the Use of the Research Passport, Misconduct in Research, Intellectual Property Management, and Records Retention are available on NHS Tayside's Staffnet, or are available on request.

 

Position Statements 

  v 2.0
          TASC CTIMP Trial Phases