Euro Roundup: EMA seeks feedback on plans to cut the clinical data needed for biosimilar approval

RoundupsRoundupsAdvertising, Promotion and LabelingBiologics/ biosimilars/ vaccinesClinical TrialsEuropeEuropean Medicines Agency (EMA)Health Authority meeting and communication strategyHuman cells, tissues, and cellular and tissue-based products (HCT/Ps)Medicines and Healthcare products Regulatory Agency (MHRA)PharmaceuticalsPharmacovigilance/postmarket surveillanceQuality Assurance and ControlRWE/RWDSwissmedic