EU calls for pharma, IVD databases to be linked

05/14/2013 | Clinica

The databases for drugs and IVD clinical-trial registration should be interoperable to streamline the process for companion diagnostics, where the two overlap, according to recommendations issued by the European Economic and Social Committee. The committee said that new regulations should ensure that the requirements and applications processes for drugs and medical devices "are compatible and reduce duplication as far as possible."

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