Meditrial
Silvia Ruggieri is a Clinical Scientist at Meditrial since March 2022, specializing in regulatory and clinical development strategies within the cardiovascular and gastrointestinal sectors, including trial design and FDA submissions. Previously, Silvia held the position of Quality Engineer at Linkverse, focusing on medical device compliance and technical documentation, from August 2020 to March 2022. As a Medical Device and CSV Consultant at PQE Group from October 2018 to August 2020, Silvia advised on quality and regulatory matters, including ISO standards and risk management. Silvia began their career at Cnim S.r.l. as a QMS Auditor, where responsibilities included QMS verification and audit preparation, and also served as a QMS Technical Officer, supporting the QA manager with SOPs and quality documentation. Silvia's experience includes an internship as a System Management Consultant, with a strong educational background comprising a Master's Degree in Biomedical Engineering and a Bachelor's Degree in Clinical Engineering from Sapienza Università di Roma.
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Meditrial
Meditrial is a leading provider of clinical trial services and digital cloud-based solutions for the lifesciences industry. As a Clinical Research Organization (CRO), Meditrial is renowned as the go-to partner by companies developing breakthrough innovations that require a clearly defined path to first-in-man and pivotal clinical studies. Established in 2008, today Meditrial is a trusted resource for large corporations as well as start-ups requiring support and resources to execute trials in the Uniteef States and Europe. Headquartered in Zürich, Meditrial has offices in Berlin, Rome, London and New York. Learm more: www.meditrial.net - www.catchtrial.com - www.mastertrial.com Despite the everchanging regulation and increasing difficulty to obtain approval for clinical investigations, Meditrial has a remarkable record of 100% success in assisting clients to execute studies in medical centers of excellence throughout Europe and United States. Meditrial's software solutions allow customers to successfully manage large global trials and registries while monitoring the results in large number of patients. Meditrial’s core strength lies in its clinical experts’ proficiency, alongside with its integrated digital platform for elearning, data capture and analytics. The organization provides a set of systems and tools to minimize complexity of clinical trials and regulatory approvals Meditrial is extremely proud to be one of the first—and very few—CROs certified by ISO 9001, ISO 13485 and ISO 27001 for information security.