07 March, 2022 - At Accellacare, we ensure patient centricity in a number of ways. All of our solutions targeted toward sites and patients have the ultimate aim of making clinical trials easier on all parties, enabling faster and more effective delivery of research studies. At the end of the day, it is about providing options for patients to access trials, and giving sites the ability to operationalise those options.
14 December, 2021 - Advances in wearables, telemedicine and remote monitoring technology along with the convenience of in-home visits were bound to make decentralised and hybrid clinical trials standard with enough time. However, the COVID-19 pandemic accelerated their adoption and now, even with the hope that the pandemic will soon be behind us, hybrid and decentralised models are poised to become viable solutions in clinical trial design because of their inherent agility, inclusivity and most importantly, patient centricity.Read more
16 November, 2021 - More so now than ever, the inclusion of more diverse, and often more relevant, study populations is gathering momentum within the clinical trial community.
From calls for more diversity in age, gender, and ethnic groups, to more consideration for lifestyle and cultural differences, trials need to ensure they represent the key population of interest and identify a greater range of opportunities to maximise benefits for both patients and pharmaRead more
10 November, 2021 - The expansion of the Accellacare Site Network increases access and engagement with investigative sites and its patients, supporting faster recruitment and reducing the overall time and cost associated with drug development for customers.
Through these new partnerships, Accellacare is also enhancing its already-strong capability in the central nervous system (CNS) and immune-inflammation therapeutic areas.Press release
3 September, 2020 - Enhances ICON’s ability to offer customers integrated solutions of patient assessments at site and in-home for decentralised trials.
Accellacare is also achieving faster study start-up for its customers through efficiencies gained in central process management including budget and contracting, which can otherwise be a source of delay. This combined with a finely tuned feasibility approach ensures that the network can identify and recruit more patients to studies, in a wide range of therapeutic areas, in a shorter time frame.Press release