We can't quite believe it's that time of year already... the first CDISC Interchange of 2018 - CDISC Europe Interchange - kicks off this week. The main conference takes place 25-26 April at the TITANIC Chaussee Berlin.
CDISC Interchanges are a great opportunity to network, learn, and uncover best practices in implementing data standards in clinical research. Regulators such as the US Food and Drug Administration (FDA), Japan Pharmaceuticals and Medical Devices Agency (PMDA), and European Innovative Medicines Initiative (IMI) require CDISC standards for submissions.
Regulatory requirements for SDTM datasets and Define.xml in submission deliverables are increasingly becoming a challenge for organizations running clinical trials. Join CEO Mark Wheeldon at the Interchange to discuss the benefits and best practices of implementing CDISC data standards across your studies.