By participating in a clinical trial you are contributing to the advancement of medical knowledge, helping to improve treatments for various conditions, and potentially providing access to new therapies or interventions.

You will be able to access real-time data via the Evripath platform with updates on your patient's clinical trial recruitment progress. The Evrima team is always available to answer any specific questions you may have.

Evrima works with leading researchers and clinicians to help make medical research breakthroughs happen and deliver better health outcomes. All clinical trials must go through an independent ethics committee review process and comply with Good Clinical Practice (GCP). Our trials span a vast range of therapeutic areas and chronic conditions. You can view our active trials here.

Evrima has advanced privacy and data protection safeguards built-in. We’re GCP Compliant, CFR Part 11 Compliant, have a robust Privacy Policy and Terms of Service.

Evrima’s Evrilink supports phase 1 to 4 clinical trials across many different therapeutic areas. Contact our team to discuss your specific clinical trial support needs, we’re here to help.

We recommend activating your Evrilink account before recruitment starts. Once we receive the green-light from you and the trial is Ethics approved, the trial can be established in Evrilink and then you can invite your sites and research partners to start recruiting for the trial. If your protocol changes, or new sites are added, these changes can be updated in Evrilink so your team has access to the latest information - in real-time.

The power of Evrilink can also be harnessed to streamline and expedite recruitment for trials that are already underway too. Contact us today to find out more.

Evrima’s Evrilink platform supports phase 1 to 4 clinical trials across many different therapeutic areas. We can quickly activate and support clinical trials whether they are yet to start or are in need of urgent support. If you aren’t sure, get in touch, we’re here to help answer your specific clinical trial questions.

Evriquest is our Marketing as a Service (MaaS) offering to help Trial Sites, Sponsors and CROs with clinical trial recruitment. Our expert team creates marketing strategies and employs targeted recruitment campaigns to reach and engage with specific patient populations, increasing the likelihood of successful recruitment for your clinical research studies.

Evriquest can benefit various types of clinical trials, including those focusing on new drugs, medical devices, treatment modalities, or disease-specific studies. Whether it's a large-scale, multi-regional trial or a niche study with a specific patient population, we can tailor a bespoke marketing strategy accordingly.

Trial Sponsors can provide a recruitment and progress update to GPs and you can also view your patient’s clinical trial journey via the secure Evripath platform.

Evrima works with leading researchers and clinicians to help make medical research breakthroughs happen and deliver better health outcomes. All clinical trials must go through an independent ethics committee review process and comply with Good Clinical Practice (GCP). Our trials span across a vast range of therapeutic areas and chronic conditions. You can view our active trials here.

Evrilink automates communication with clinical trial participants so they are kept informed when they are referred, withdrawn or disqualified from the recruitment process. Better communication, delivers a better clinical trial experience for the participants and reduces the workload of clinical trial teams.

Sites and Sponsors have real-time access to enterprise level reporting so they are able to access recruitment progress when they need to. Clinical trial sites no longer need to provide pre-screening logs in email or spreadsheets, and Sponsors or CROs no longer need to collate multiple sources of data across their different sites.