EIPG: Guidelines open for consultation and coming in force, and a webinar on microbiome
Open consultations include the Discussion paper on patient disease registries, the guideline on the environmental risk assessment of medicinal products for human use and EMA's strategy on Regulatory Science to 2025. The guideline on the Trial master file will come into force on 6th June 2019. The webinar of 17th June will focus on the microbiome and stress–related psychiatric disorders
