Top Quality Documents

Solutions for Quality Documentation




Louise Perry, BSc Hons Physiology & Biochemistry 

Louise Perry

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 trials.


Additional responsibilities within Top Quality Documents include development and maintenance of Standard Operating Procedures and taking the lead for improvement of internal company processes. 

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