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Expert Opinion on Drug Safety|October 15, 2021
Improving the data quality of spontaneous ADR reports: a practical example from MaltaMarta Zuccarelli, Benjamin Micallef, Dianne Butler, et al.
Expert Opinion on Drug Safety|April 12, 2021
Regulatory experience of handling Risk Management Plans (RMPs) for medicinal products in the EUDianne Butler, Katarina Vucic, Sabine Straus, et al.
Drug Discovery Today|May 21, 2022
Outcomes and endpoints in clinical trials supporting the marketing authorisation of treatments in paediatric acute lymphoblastic leukaemiaBenjamin Micallef, Robert Nistico, Ole Weis Bjerrum, et al.
Drug Discovery Today|January 10, 2022
The changing landscape of treatment options in childhood acute lymphoblastic leukaemiaBenjamin Micallef, Robert Nisticò, Sinan B Sarac, et al.
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