Laura joined the ESPL team in 2023. Laura has over 10 years regulatory experience in both industry and consultancy, and a First class honours degree in Biomedical Science. Laura is a senior consultant and supports preparation and coordination of MA submissions, via National, Decentralised and Mutual Recognition procedures, clinical trial applications, as well as development activities such as scientific advice, …

Kirsty is a member of the ESPL publishing team having originally joined as our Company Administrator. She supports the submissions team in preparing esubmission documents for inclusion in eCTD sequences, NeeS, etc. and uploads via agency portals.

Eleanor has recently moved into the regulatory team, having joined as a member of the ESPL publishing team straight from university, whereshe obtained a First Class honours degree in Neuroscience.  Eleanor support various regulatory activities including MAA and lifecycle activities, RMPs and orphan designation applications.

Tony was a founding Director of ESPL. Following an academic career at Loughborough University and then at Manchester University, in electronics and electrical engineering, Tony moved over to working independently, initially contracting to major electronics companies such as Philips, Siemens and V-Tech and developing embedded signal software applications for other clients. Tony is Chairman of Employee Ownership Trust, a member …

Ian joined ESPL in 2017 after graduating with a degree in Chemistry with Medicinal Chemistry from the University of Glasgow. Ian is a Regulatory Consultant on the team and supports OTC, orphan drug and new innovation projects. Ian also coordinates all of the PIL user testing for clients.

Anna is the Company Administrator, based in Shetland. She provides administrative support to the Board Directors, manages the company’s quality management system, and is PA to Helen and Jason.

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.

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