The MHRA has replied to the Concept Paper on the revision of the Clinical Trials Directive and it can be seen at the following site: http://www.mhra.gov.uk/home/idcplg?IdcService=SS_GET_PAGE&ssDocName=CON120341
- Risk Management in Early Phase Clinical Trials
- Faculty conversation: TQT study – this is the end!
- EUFEMED Joint Conference of European Human Pharmacological Societies 2015
- EUFEMED consultation response to EMA Draft proposal for an addendum, on transparency, to the ‘functional specifications for the European Union (EU) portal and EU database to be audited’
- EUFEMED – Joint Conference of European Human Pharmacological Societies 2015