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Pre-approval clinical trials cannot possibly ensure that a drug will not have disastrous side effects once it arrives on the market. Post-approval safety data gathering was put in place to address this problem, but as implemented, it has not proven to be as effective as hoped. This is due to the fact that, current post market safety studies largely depend on the submission of spontaneous case repo ...

Description AALIANCE2 is building further upon the AALIANCE Innovation platform (2008-2010) to:1. Transform the existing AALIANCE Community in a long-term sustainable network:a central 'meeting point' for Ambient Assisted Living (AAL)-related issues and stakeholders in Europea European Technology Platform on integrated solutions for the soci ...