TASC Policies




Drug Accountability in Clinical Trials of Investigational Medicinal Products
Pharmacovigilance and Safety Reporting
Clinical Research Quality Management System
GCP Monitoring policy
Good clinical practice training policy for personnel involved in clinical research  
TASC publication policy: guidance for trialists
Negotiation and Signatures of Agreements of Investigator-led Clinical Trials Sponsored by University and/or the Board
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 

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          TASC CTIMP Trial Phases