We are rapidly approaching the halfway point for EMA assessment. Over the next few weeks there will be a bit of activity in the EU regarding the Vitrogro assessment and so we get some sence of movement I will post the activities which should be going on.
Today the Committee for Medicinal Products for Human Use (CHMP) rapporteurs (the guys responsible for the assessment of Vitrogro) are due to submit their assessment reports to CHMP.
Don't expect an announcment about this as it is just part of normal EMA procedure and they wopn't be communicating with either BSI or TIS about this.
Rev
We are rapidly approaching the halfway point for EMA assessment....
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