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2018 Abstracts to the Programme

Patient-generated health data (Social Media) is a potential source for ADR reporting click here


 Practical application of the EMA 0070 Policy on publication of clinical data for medicinal product for human use click here


 The Evolution of Personalised Health Care within Data Management? click here


 30 years of drug coding, where are we now? click here


 SDV in Risk Based Monitoring, including quantitative experience click here


 Electronic Health Records (EHR) as eSource in Clinical Trials click here


 When the subject becomes the investigator – a paradigm shift driven by technology ?! click here


 Operational Efficiency Across the Study Lifecycle click here


 EHR for clinical studies click here


 RBM Trek (Case Study in Risk Based and Central Monitoring Implementation) click here


 7 steps to implement GDPR successfully click here


 Handling the increasing volume and complexity of external data in Clinical Trials in Data Management click here


 Scaling up the trustworthy reuse of EHRs for clinical research click here


 Digital initiatives and potential impact on the Data Management click here


 Status of the life sciences industry today, impact on sponsor-CRO relationships and on day-to-day work in clinical research click here