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Our computing systems are designed to meet the specific requirements of PHRU's new and on-going studies and to ensure that they are sufficiently adaptable to provide a platform for future work. Our systems focus on aspects that are key to study quality: recruitment of large numbers of eligible participants; data collection and study conduct; study management, coordination and oversight; laboratory management including analysis and storage; ascertainment, confirmation and classification of outcome; and analysis, reporting and dissemination.

Our bespoke IT systems comply with relevant security and data privacy policies and regulations (including EU Data Protection Directive 95/46/EC, and US Health Insurance Portability and Accountability Act (HIPAA) 1996) as well as, where appropriate, standards for clinical trial systems (including US Code of Federal Regulations Chapter 21 Part 11 “Electronic Records and Signatures” and EU Clinical Trials Directive).

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