• The newest developments in the requirements on clinical trials registration from International Committee of Medical Journal Editors, industry associations and upcoming legislation (globally)
• Challenges with managing the ever growing clinical trial registration requirements and the amount of information that needs to be compiled in order to stay compliant and up-to date
• Demonstration of the front-end public accessible clinical trials portal
• Presentation of PURE - a new standard IT system centralising public clinical trial information
• How to deal with the challenges of improving the workflows for trial information gathering and increasing transparency within the pharmaceutical organisation

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