Top Quality Documents

Solutions for Quality Documentation

 

 
 

Profiles

Sarah Mewett, BSc Hons Pharmacology

 
Sarah Mewett

Sarah has a comprehensive knowledge of pharmaceutical research and development, having worked in the industry at different stages of the R&D process for over 25 years. Before the founding of Top Quality Documents in 2001, Sarah worked as part of a multinational team setting up clinical trials for a large pharmaceutical company, culminating in the production of study reports or in some cases New Drug Applications. Subsequently she focussed her expertise on the quality aspects of clinical documentation while undertaking smaller writing projects.

 

More recently Sarah has been involved with the validation of subject data within ongoing clinical trial databases for interim data-cuts and regulatory reporting.

 

Additional responsibilities within Top Quality Documents include the development of a management tool to track multiple work-streams ensuring timelines and budgets are met along with all aspects of the company’s financial arrangements, both with clients and in-house.

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