Dossier Compliance – Study Reviewer

Eileen has over 30 years’ experience in toxicology gained at the world renowned Central Toxicology Laboratory within ICI, Zeneca, AstraZeneca and Syngenta. For the past 15+ years she has worked as reviewer within the Human Safety Group drafting regulatory summaries, populating regulatory submission dossiers, reviewing data to provide the basis for rebuttal statements, preparing competitor reviews, writing toxicology reports and auditing studies for compliance with GLP.  Her expertise includes the ability to abstract, collate, interpret and summarise data and to present it in a format that meets the requirements of international submission dossiers.  More recently Eileen has gained exptensive experience of IUCLID Robust Summary compilation.

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