For patient organisations
Bring clinical trials closer to your community
Your own trial portal on your website, free of charge, plus practical support to help your members understand clinical research: education, social media material, webinars, patient stories, and reports that help you prepare for new treatments in your disease area.
How we support your organisation
Everything is shaped with you, in your style and your members' languages.
Free trial portal
Your own trial portal, embedded free on your website
A version of the TrialsConnect search tailored to your disease area and your community, carrying your name and style. Your members find trials without leaving your website.
- White-label: your logo, colours and wording.
- Trials in your disease area from EU CTIS and ClinicalTrials.gov, with status confirmed by the centres where available.
- Plain-language summaries in your members' languages.
- Embedded free of charge. Your organisation stays data controller; Esperity works for you as processor.
Trial awareness education
Education packages that build confidence
Ready-made modules help your members understand what taking part in research means, so they can have a better conversation with their doctor.
- What a clinical trial is, how phases and randomisation work.
- Rights and safety: consent, ethics review and the right to stop.
- Questions to bring to the doctor, and how to use your trial portal.
- Videos, leaflets and e-learning, reviewed with patient representatives and clinicians.
- What is a clinical trial? Phases, randomisation, placebo
- Your rights and safety Consent, ethics committees, stopping at any time
- Talking to your doctor Questions to bring to the consultation
- Finding a trial How to use your portal
- Short videos
- Leaflets
- E-learning
- Your languages
Social media and webinars
Material for your channels, and webinars your members can join
We help you design social media content and organise webinars on trial awareness, so the message reaches your community where they are.
- Posts, carousels and short videos designed in your organisation's style.
- Campaigns around awareness days or the launch of your portal.
- Webinars with clinicians, research nurses and patients who took part, with time for questions.
- Recordings you can share with members afterwards.
With a clinician, a research nurse and a patient who took part
Patient stories
Help members share their experience of research
Personal stories make clinical research easier to understand. We help you collect and present them carefully.
- Interviews and short written or video testimonials.
- Written consent, approval before publication, and the right to withdraw.
- Factual and non-promotional: no medicine or sponsor names.
- Stories stay the property of your organisation and the people who share them.
Preparing for new treatments
Be ready when new treatments come to your disease area
Periodic outlook reports show which trials and treatments are moving forward in your disease area, so your organisation can prepare to bring the patient perspective at the right time.
- Late-stage trials and treatments under regulatory review, from public sources.
- What patient evidence may be relevant: experiences, unmet needs, preferences and quality of life.
- When to engage, and how to gather this information from your members in a careful, structured way.
- How to work with sponsors transparently: written agreements, independence and public disclosure.
- Late-stage trials in your disease areapublic registries
- Treatments under regulatory reviewpublic sources
- What patient evidence may be neededexperience, preferences
- How to work with sponsors transparentlyagreements, disclosure
How we start together
Listen
We learn about your members, the questions they ask and the languages they use.
Set up your portal
We tailor the trial search to your disease area and style, and you embed it on your website.
Choose your support
Education, campaigns, webinars, patient stories or outlook reports, as and when they help you.
Grow awareness
Your members find trials and understand research better, in a place they already trust.
Your organisation stays independent
Your voice, your community, your decisions.
- You decide what appears on your portal and in your materials.
- Information, not advice: everything helps members prepare a conversation with their doctor.
- No promotion of medicines, and no sponsor can pay for a higher position.
- Any sponsor collaboration follows written agreements and is disclosed in line with the applicable codes of practice.
- Patient stories only with written consent. No patient data is collected through the portal.
Let's talk about your community
Tell us about your members and the questions they ask. There is no obligation.