Vault CTMS system will enable SGS to share with its clients the state-of-the-art reporting capabilities and deliver greater flexibility in running studies. Together with Veeva Vault eTMF (electronic trial master file), SGS will drive greater harmonization across its clinical operations. SGS will begin running studies on Vault CTMS in spring 2019, with any current studies scheduled to end after June 2019 being migrated to the new system.
"Veeva Vault CTMS, along with Veeva Vault eTMF will allow us to streamline our clinical trial management and improve decision-making within our planning and operations teams across the Americas and Europe," commented Janelle Johnson, SGS International Project Management Director. "SGS is committed to investing where necessary to maintain its leadership position in clinical research, and ensuring it can have the most efficient systems, and in-turn, offer the highest level of service and experience to our clients."
"Veeva Vault CTMS will enable SGS to improve its operational efficiency and drive faster, higher-quality trial execution" said Henry Galio - Senior Director, Veeva Vault CTMS. Now clinicians and managers can have greater oversight and improved decision-making capabilities during studies".
SGS Life Sciences provides clinical research, bioanalytical, biologics characterization, biosafety, and quality control testing. Delivering solutions in Europe and the US, SGS offers clinical trial (phase I to IV) services encompassing clinical project management and monitoring, biometrics, PK/PD modeling and simulation, and regulatory and medical affairs consultancy. SGS has its own clinical unit in Belgium and two phase I patient units based in Belgium and Hungary. SGS has a wealth of expertise in first in human (FIH) studies, human challenge testing, manufacturing challenge agents, biosimilars and complex PK/PD studies with a focus on infectious diseases, vaccines and respiratory therapeutics.
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