Louise's pharmaceutical industry experience spans more than 30 years,
including roles in clinical research with international pharmaceutical companies and a
contract research organisation. She is experienced in the conduct of phase I to III hospital
studies as well as later phase studies in general practice.
Prior to the formation of Top Quality Documents, Louise held a senior role
within the quality review department of a blue chip pharmaceutical company, contributing
towards the introduction of quality review procedures across clinical project teams and
ensuring consistent and timely reviews. In addition to quality review assignments for
regulatory documents, Louise also undertakes data validation projects for ongoing clinical
Additional responsibilities within Top Quality Documents include development
and maintenance of Standard Operating Procedures and taking the lead for improvement of
internal company processes.