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We're changing the face of clinical trials using smart, randomized trial design

Our streamlined approach and scalable digital infrastructure transforms the way randomized controlled trials are conducted. We work together with our partners to generate robust evidence for new treatments at a fraction of current industry costs. This helps us to reduce the barriers in the development of and access to better treatments for common diseases.

A truly integrated approach

We are driving change in the design, management and delivery of clinical trials. By having the right partnerships, systems, processes and capabilities in place, we can deliver definitive, streamlined and cost effective clinical trials.

 

We work closely with our partners from start to finish. Together with them, we design and manage smart, highly efficient trials that combine the fundamental principles of randomization, with advances in health data and technology. We  involve the clinical and patient communities that participate in our trials or stand to gain from the results they generate. We work closely with regulators and others to ensure that our trials deliver results that facilitate prompt licensing, market access and purchasing decisions.  Together, this ensures our trials provide robust evidence for treatments with huge potential impact on health.

Each trial is tailored to meet the specific scientific, regulatory, clinical, and patient needs. Trials are developed and delivered using a quality-by-design approach that considers the full life-cycle of each trial from planning and recruitment to generation of robust and relevant results for regulatory, payer and clinical decision-makers. The operations are underpinned by our flexible, secure, standards-based IT platform that can be tailored for each individual protocol and make appropriate use of routine health data and patient-centered technology. We use statistical and risk-based approaches to monitoring and quality management to improve results and significantly reduce trial costs.

Through this integrated approach, we aim to vastly improve the pipeline of treatments for common diseases.

Trust and transparency

Earning and maintaining trust is core to our work. We are committed to using data safely, responsibly and in accordance with all relevant ethical and legal requirements. We are dedicated to acting responsibly and demonstrating that we do so through involvement and engagement of trial participants, patients, and the wider public.

Patient and public engagement

Patients and the public provide valuable insights into the design and delivery of clinical trials, helping to ensure that the results and their application to medical practice meets their needs. We will be forming a Patient and Public Involvement and Engagement Panel in the coming months to inform the design of our  studies.

Collaborate with us

We are interested in opportunities to partner with pharmaceutical companies, biotech, academic research teams, healthcare providers, charities and investment organisations that share our mission to accelerate the adoption of novel treatments through robust randomized controlled trials.

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Latest news & stories

Corporate 12 July 2022

Funding announcement: Protas receives support from Schmidt Futures

Protas announces today that it has been awarded a $2m USD grant by recommendation of Schmidt Futures, a philanthropic initiative…

Corporate 20 May 2022

International Clinical Trials Day

Today is International Clinical Trials Day- a day to recognise the importance of good clinical trials for public health. We…

Corporate 11 May 2022

UCTMP Procurement

Protas has recently released a contract notice for a Unified Clinical Trials Platform (UCTMP).

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