Bridging Patients and Industry
We believe that clinical trials should be transparent, inclusive, and understandable.
Our mission is to give patients a clear understanding of trial documentation through comprehensive reviews and structured input from the public and patients.
Who is this service for?
Whether you are working to make patient-facing information more accessible, seeking clarity as a patient, or advocating for better systems — we are here to support you.
Companies &
Industry Leaders
Patients &
Community Reviewers
Patient Advocacy Groups &
Strategic Partners
Accelerate Trust and Transparency
We help industry partners improve the
clarity and accessibility of trial documentation.
Collaborate with us to ensure your
materials meet patient needs and
regulatory expectations.
Discover how we support companies.
Be a Voice for Clarity in Clinical Trials
Are you a patient, carer, or someone who just want to make a difference? You can help make clinical trial information clearer and more accessible. We invite individuals like you to register your interest in
becoming a reviewer of patient-facing documents.
Your insights help ensure that trial materials are understandable, respectful, and truly
patient centred.
Register to become a patient document reviewer.
Amplify Voices, Drive Change
We work with advocacy groups and strategic partners to gather structured input from the public and patients. Together, we shape trial documentation that reflects real-world needs and values.
Linguistic, patients and community
reviews, for ethics ready reports
Patient-facing materials will receive a readability review, basic editing. A recorded interview with guided questionnaire, with transcripts provided if necessary.
We also offer a bespoke Language review. Bespoke questionnaire / interview
Key Benefits
Simplicity is a benefit...
- Patients and community members review of patient-facing materials with written recommended updates in as quick as 7 days
- Language reviews with analytics and recommended changes overseen by our certified linguist
- Meeting patient involvement government requirements
- Clear pricing
- Small company agility
Key Stages
Faster Ethics Approval – Fewer revisions, quicker decisions.
Enhanced Recruitment Materials – More engaging and understandable.
Improved Ethics Submission – Stronger, patient-informed documents.
Review of Materials – Real feedback ensures clarity.
Earlier Trial Launch – Everything ready, faster.
How Patient Reviews Accelerate Clinical Trial Start-up
1. Faster Ethics Approval
Clearer Consent Forms: Patient-reviewed documents are more readable and aligned to ethical standards, reducing back-and-forth with ethics committees.
Validated Feedback from Community Members: Demonstrates due diligence and participant-centred design, which can streamline approvals.
Fewer Revisions: Ethics boards are less likely to request changes when materials are already tested with real patients.
✅ Result: Ethics approval can be granted in fewer rounds, saving weeks delay
2. Improved Recruitment Materials
Language that resonates: Patient-reviewed materials speak directly to the target population, increasing interest and trust.
Reduced Confusion: Clearer information means fewer questions and hesitations from potential participants.
Higher Conversion Rates: More people who read the materials go on to enrol.
✅ Result: Recruitment starts sooner and progresses more smoothly.
3. Fewer Protocol Amendments
Early Identification of Misunderstandings: Patients flag unclear or misleading content before launch.
Prevention of Dropouts: Better understanding leads to more informed, committed participants.
✅ Result: Fewer mid-study changes, which are costly and time-consuming.
4. Audit-Ready Documentation
Structured Reports: Patient feedback is documented in a format that supports regulatory review.
Transparency: Demonstrates a proactive approach to participant engagement and inclusion.
✅ Result: Less time spent preparing for audits or responding to regulatory queries.
Empowerment Through Understanding
Empowering patients means providing them with clear insights on trial documentation.
We review patient-facing materials for comprehensiveness.
Connecting public and patients allows us to gather structured feedback.
At PatientViewonline, we believe patients deserve more than access — they deserve clarity, respect, and a voice. We transform complex clinical trial materials into clear, compassionate content co-created with patients, so they can truly understand, engage, and shape the future of medicine.
Because better communication leads to better research— ensuring better outcomes for everyone.
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