Clinical Trial Management

PRN Services

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 us and made PRN the success that it has been over the last 23 years.

Contact Us TodayOur Services

What We Offer

Our Services

Comprehensive clinical trial management solutions tailored to your specific needs

Project Management
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.
Regulatory Affairs
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.
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.
Clinical Monitoring
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.
Safety
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.
Data Management
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.
Biostatistics
Full statistical support from the concept stage (sample size calculations). Provision of statistical analysis plans, generation of Tables, Figures and Listings, and incorporation of statistical analysis data into the study report.
Consultancy Services
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.

Our Track Record

Facts & Figures

0

Studies Completed to Date

0%

Of Trials Completed to Time and Budget

0

Patients Recruited

0

Countries

Get In Touch

Contact Us

Contact us today to discuss how we can support your next project

Let's Start a Conversation

Whether you need full clinical trial management or specific consultancy services, our experienced team is ready to help. Reach out to discuss how PRN can support your clinical development goals.

Office

United Kingdom