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Pharmaceutical Manufacturing and Packing Sourcer

A Seamless Supply

Clinical trials can vary in their scope and design and can be either single-site or multi-site, happening in a single country or in several geographical areas. In some clinical areas, studies are becoming larger and more complex, while the sponsors desire faster recruitment and data generation. Multi-site, multi-country studies are challenging as they require the coordination of many different parameters such as manufacturing, packaging, temperature management, storage, and distribution.

Clinical trials usually comprise three different stages: the study preparation, the active study (between ‘first patient, first visit’ and ‘last patient, last visit’) and the finalisation of the study (after ‘last patient, last visit’). Each of these stages will face different challenges of the logistics and supply chain that must be controlled.

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Celine Chanforan graduated with a Masters in Food Science from the University of Montpellier, France, in 2006, and achieved her PhD in Food Chemistry from the University of Avignon, France, in 2010. Celine started her career as Project Manager in the food ingredient sector for nine years. Celine mainly managed R&D projects for food colours and dietary supplements. After moving to the UK in 2016, Celine has been in charge of projects related to the delivery of new immunoassay tests for various applications and in accordance with in vitro diagnostic quality management system ISO 13485. In 2017, Celine joined Onorach as Clinical Project Manager and is now in charge of the international clinical project portfolio.
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Celine Chanforan
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