Boost the impact of your clinical trials and expanded access by making them more accessible to patients and physicians.
Clinical trials
We support patient access to clinical trials globally. Backed with the latest developments in technology and innovation, we aim to improve access and participation in clinical trials.
We create tailored clinical trial awareness campaigns and have relationships with key physician networks and patient advocacy groups within our focus areas through our Medical Community team.
We connect all relevant parties in clinical trials, streamlining recruitment activities and support on one platform.
Our medically trained Patient Navigators pre-screen patients and compliantly collect the relevant medical information to reduce site screening burden.
Our platform and solutions strictly adhere to GDPR regulations and meet ISO-27001 standards for data security and privacy.
myTomorrows can support your patient recruitment activities, from patient awareness to site referrals. With experience in many therapeutic areas, including rare diseases, hematology, and oncology, we are best placed to help you meet your goals.
Expanded Access Management and Real-Word Data
Benefit from our decades of experience for tailored expanded access programs that support clinical development goals.
Physicians are guided through the whole EAP application process by experienced site managers and a user-friendly digital platform.
Our team of specialists is a front runner in gathering evidence from real-world data collected within an expanded access setting.
We hold quality certifications, regulatory licenses, and provide global regulatory services.
Building on our extensive experience in EAP management and global EAP coverage, myTomorrows can support you with tailored EAP programs that align with your clinical development goals.
Discover how our comprehensive omni-stakeholder solution supports BioPharma organizations globally to meet clinical development goals.
We have a full range of awareness tools and can offer pre-screening solutions, supported by state-of-the-art technology. This allows for timely engagement of sites with patients and their physicians, and the continuous sharing of high-quality referrals to trial sites.
Our platform enables expanded access processes, including the possibility for patients and physicians to upload application documents securely on the platform. Additionally, myTomorrows’ fit-for-purpose EDC can be tailored for specific use cases according to client needs.
Our platform is fully ISO 27001-certified and GDPR-compliant, allowing for secure and compliant data exchange in clinical trial and expanded access settings. This approach streamlines patient-trial matching and, in select instances, also allows for compliant reporting on the clinical trial recruitment funnel.
We’ve combined some of our most asked questions to help you get started. You’ll find more on our FAQs page, however, don’t hesitate to get in touch if you have more specific requests.
