Summary
Task 132 Determine requirements for ADDIS uptake within HTA agencies regulatory bodies and industry M1M12 UMCG Astellas Amgen ZINPilot projects will be performed with key partners to determine the requirements for ADDIS to become part of the process of analysing the relative effectiveness of drugs and of communicating these analyses and their results Testing will take place both with regulators such as MEB HTA parties such as ZIN and industry partners such as Astellas and a discussion is running with Novo Nordisk pharmaceutical companies and Pharmerit an international research service provider D115 Examples of requirements could be a private installation process within an organisation for sensitive data or a specific import or export format to better connect to the databases of a company or institution We will also attempt to set up a collaboration with the MAGIC organisation to allow ADDIS network metaanalyses to be used in their tool
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