Has been working within the regulated pharmaceutical IT environment since 1994. Trev has held a variety of roles within the Pharmaceutical Industry from IT Developer, Project / Validation Manager through to Quality Management and Quality Assurance, working across GLP, GMP, GCP and GPvP at both a local and global scale. As an IT Quality Assurance auditor, Trev has experience within the USA, Europe and Asia for Clinical suppliers such as CROs, Analytical and Clinical Laboratories, Electronic Data Capture providers (Patient Diaries, IVRS and IWRS), and medical imaging (ECG, Ultrasound).

Trev is the lead consultant for our Pharmaceutical IT Quality Assurance and Computer System Validation activities.

Has been working within regulated pharmaceutical IT environment since 1995 in variety of roles including;
· Business process review. Using previous experience Debbie is able to advise on process improvement from simple but overlooked smarter working to complex improvements involving use of your company’s current and new technologies, always with a structured quality and audit sound strategy underpinning implementations.
· Information Protection, where she was a key lead in rolling out information protection strategy in one of largest pharmaceutical companies globally
· IT support and development
· Training
· Web design

Debbie is the lead consultant for our Web Design and Process Analysis activities.