Bridging Patients and Industry
Our mission is to give patients a clear understanding of trial documentation through comprehensive reviews and structured input from the public and patients.
Linguistic and patient/layperson review, for ethics ready reports
Patient facing material 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...
- Real layperson or patient reviews of patient facing material 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 Lay Feedback: 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—and ensuring better outcomes for everyone.
©Copyright. All rights reserved.
We need your consent to load the translations
We use a third-party service to translate the website content that may collect data about your activity. Please review the details in the privacy policy and accept the service to view the translations.