Experience As Required
PRN have been providing clinical trial management services since 1999. With an average of 26 years experience at the senior team level we possess a wealth of knowledge in managing Phase I-IV global studies. PRN work to core values built around integrity, creating talented and dynamic teams, exceeding quality expectations and to always listen to what our clients are asking. These values have underpinned and made PRN the success that it has been over the last 23 years.
Contact us today to discuss how we can support your next project.
DISCOVER OUR EXPERTISE
At PRN we maintain strong strategic planning, close attention to detail and robust communication processes with an extensively experienced team implementing rigorous project planning whilst delivering the highest quality service
Given the rapidly changing regulatory landscape and the greater complexity of clinical trials we partner with experts who are continually involved on the latest developments in this field. We have formed a tried and tested collaboration with a long established Regulatory Affairs consultancy and find that provision of a mixture of specialist advice and ‘hands on’ compilation of regulatory dossiers works well for our Sponsors
Feasibility & Protocol Development
Critical to any study success is establishing robust pre-study site feasibility data. In addition to the all important patient numbers is a full understanding of the site's ability to manage the study, apply their expertise and provide any support services needed. PRN draw on over 26 years experience in the development of study protocols compiled by our Medical Writers
The Clinical Research Associate role is pinnacle to the successful collection of accurate study data. We consider our CRAs as the eyes to the study source data and critical in the oversight of the study at the local site level. It is why we only recruit experienced CRAs who are fully supported via our ‘hands on’ management approach incorporating a comprehensive co-monitoring policy to continually review and support activities at study sites.
Provision of a full range of Pharmacovigilance support services from collection of safety data in a validated Argus database through to completion of PSUR and DSURs, signal detection and provision of a QPPV
Provision of full data management support utilising third party validated EDC systems. CRF design, data monitoring, data entry, incorporation of QOL assessment and imaging data, integration of data from external databases (e.g. central labs)
Full statistical support from the concept stagge (sample size calculations). Provision of statistical analysis plans, generation of Tables, Figures and Listings, and incorporation of statistical analysis data into the study report
We understand that many of our clients might be at the very early stage of development or do not require a full service offering. PRN can provide a fully flexible approach to their clients needs and adapt as these requirements change. Whether it be provision of clinical trial management support or study monitoring we can identify a bespoke solution that fits best.
Facts & Figures
STUDIES COMPLETED TO DATE
OF TRIALS COMPLETED TO TIME AND BUDGET
Grove House, Lutyens Close, Chineham Court,
Basingstoke, United Kingdom