ESPL is excited to announce the launch of its new website. With the support of Highlands and Islands Enterprises (HIE), ESPL has worked with Denvir Marketing to create a new website to provide visitors with a modern, easy-to-navigate, overview of our company and services. As we know, in this connected-technology era, having a website that provides clear and insightful information …
ESPL are seeking a Regulatory/Medical Writer, based in Ireland or the UK, to join the team and work alongside the Senior Management Team and Consultants in supporting the document writing activities of the ESPL team. This permanent role will include: Preparation of documents to support regulatory activities at various stages of pharmaceutical or medical device development, such as : Clinical …
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Stefania joined ESPL in 2011 and supports directing, managing and coordinating European MA submissions, via National, Decentralised and Mutual Recognition procedures. She also provides expert support to clients on Module 3 (Quality) regulatory requirements for sterile products. She has a PhD in Biochemistry and lives in the mountains near Milan with her husband and daughter.
Dolores has been working with ESPL since 2011 and provides a broad range of consulting support. She has supported submissions for STED filings for medical devices, ASEAN CTD dossiers, EU MA filing, and Regulatory strategy. Dolores has been working in Regulatory Affairs for over 20 years and has a PhD in Medicinal Chemistry.
Diane is ESPL’s submissions manager and is responsible for overseeing all publishing activities. ESPL’s publishing services include preparing PDF’s, formatting documents, tracking projects, and compiling eCTD submissions, as well as supporting other format submissions. Diane has degrees in Chemistry and Computing and IT.