Top Quality Documents was established in 2001
by former members of a dedicated review group within a leading global pharmaceutical company. We are a team
of trained reviewers based near London, and are able to support clients anywhere in the UK and abroad. We
provide an alternative service to clinical research organisations which is cost effective and
We can work independently or as a collaborative team, enabling us to take on
larger projects and still meet the all too frequent, tight timelines associated with regulatory submissions.
Top Quality Documents associates all have extensive experience in reviewing regulatory documentation, and in
the drug development and submission process.
For more information about what we do, please see our services page.
Brief summaries of our associates' experience can be found below: