Online Training Repository
Randomisation – the method by which participants are randomly allocated to treatment groups – is…
This talk investigated the statistical design features of a breast cancer risk reduction Bayesian adaptive…
Informed consent is considered a fundamental requirement for participation in trials, yet obtaining consent is…
At the 2015 REWARD/EQUATOR conference on research waste, the late Doug Altman revealed that…
HRB-TMRN, UCC & TMRP Study Day Annabelle South is the Policy, Communications and Research Impact…
HRB-TMRN, UCC & TMRP Study Day Simone holds an MSc in biology from Texas A&M…
HRB-TMRN, UCC & TMRP Study Day Ellen is a PhD student with the HRB-TMRN based…
HRB-TMRN, UCC & TMRP Study Day Heather has been a public research partner in research…
HRB-TMRN, UCC & TMRP Study Day Katie Gilles is the Director of the Health Care Assessment Programme and…
HRB-TMRN, UCC & TMRP Study Day Eleanor Mitchell is an Associate Professor of Clinical Trials…
HRB-TMRN, UCC & TMRP Study Day Fiona is Programme Manager for the HRB Clinical Trials…
Regulators are promoting innovation to speed up drug development. Subsequently, there is increasing interest in…
An overview of four studies-within-a-trial (SWAT) was presented – completed as part of the Cognitive…
HRB-TMRN & RCSI Study Day Anne-Marie Byrne is the Programme Manager for the National Surgical…
HRB-TMRN & RCSI Study Day Declan is the Chair in Health Research Methodology and Deputy…
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