Patient focused research for better outcomes
Avoid the risk of clinical trial disruption while protecting patient safety by deploying in-home and alternative site solutions.
Monitoring strategies based on risk analysis and assesment for more resilient operations.
Decentralised and hybrid clinical trials have been prevalent for years, yet sponsors have struggled to execute these patient-centric trials effectively. Explore the perceived barriers and how you can make these models a feasible option for the future.
Read the whitepaper
What does the patient want? In 2019, ICON conducted a web-based survey through its global research site network, Accellacare, to get the patient view and learn whether bringing the trial to the patient makes a difference in accessing more patients. With over 4,000 patient responses, we explore perceptions and preferences around what makes it easier for patients to participate in clinical trials and to determine whether industry perception was reality.Read the report
The COVID-19 outbreak has driven the desire for more resilient clinical trials. The deployment of remote clinical monitoring is proving its value in helping to keep trials going at a time when site management is particularly challenging. But realising this transformation requires a flexible mindset, investment in new technologies and close collaboration between stakeholders.Access the webinar recording
Although mHealth devices and sensors are continuing to evolve, and it is now possible to capture a vast array of physiological data, the operationalisation of digital trials is not without challenges. Navigate the shift from traditional trial models to agile, patient-centric processes driven by digital health technologies.Read the whitepaper
During COVID-19 the levels of remote monitoring increased due to site closures and safety reasons. Now is the time to learn from that experience and review whether a hybrid model of remote monitoring and centralised monitoring is the way forward for some trials. Learn best practices in analysing and assessing risk in clinical monitoring and how to remain agile adapting to environmental conditions and therapeutic focus.Read the whitepaper
Bringing the trial to the patient:
Understand how to implement wearable devices and harness digital endpoints in clinical trials:
The collection of real-time data in a home setting can give sponsors and trial managers greater visibility and assurance around GCP and protocol compliance.
How to best incorporate digital endpoints at every stage of clinical research.
Choosing the best option for your clinical trial.
Wearables are improving the clinical trial experience for patients and satisfying the need to collect data for real-world use studies.
Starting clinical trials in weeks, as opposed to months, should be possible post-pandemic.
Reducing the burden that clinical trial participation places on patients can help to keep patients engaged in clinical research.
Seven steps to closing the gap between rhetoric and reality in patient-centricity.
Exploring the patient perspective from different angles.
Steps to implement security into mHealth development.
Patient engagement is permeating all spheres of the healthcare ecosystem.
Revolutionising clinical trials with wearables and digital endpoints.
Project teams need to be challenged constantly to justify the study procedures and eligibility criteria they are proposing.
How can pharma improve the patient centricity of its trials during COVID-19 and beyond?
Decentralised and hybrid trials bring a wide range of benefits to the patient and the sponsor. Find out more about the range of decentralised and hybrid trials services available from ICON.Read more about ICON's services