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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