Medical writing
Which document keeps coming back?
Lay summaries, patient information and consent forms go back through review for clarity issues a tool could have caught first. HealthLiteracyCopilot scores each draft and suggests plain edits with citations to your sources. It keeps protected terms and approved disclaimers word for word, so reviewers see only what changed.
For heads of medical writing and plain-language summary leads
HealthcareGPS is SOC 2 Type II audited and HIPAA compliant. How we protect your documents
What you check first
Changes your MLR reviewers can follow
- Product names, safety language and approved disclaimers kept word for word.
- Every change tracked with its reason.
- Suggestions drawn from your approved sources, each with its citation.
Illustrative example, with a synthetic portrait.
What you're measured on
Open a measure to see why it matters and how HealthLiteracyCopilot helps.
Review rounds
- Why it matters
- A draft that comes back for clarity issues costs another MLR round and more reviewer time.
- How HealthLiteracyCopilot helps
- Each draft is scored and gets plain edits, cited to your sources, before review. Every change is tracked with its reason, so reviewers see what changed and why.
We don't promise fewer rounds. The review workload calculator shows what your current rounds cost.
Cycle time
- Why it matters
- Under the EU Clinical Trials Regulation, lay summaries are generally due within 12 months of the end of a trial.
- How HealthLiteracyCopilot helps
- Protected terms and approved disclaimers are kept word for word, so reviewers see only what changed.
We don't promise a cycle time.
Lay-summary output
- Why it matters
- Each EU trial needs a lay summary written for the public, and each one goes through review like any other document.
- How HealthLiteracyCopilot helps
- Each lay summary is scored against your target grade and PEMAT. Plain edits come from your approved sources, each with its citation.
Your writers and reviewers still approve every summary.
Why plain language matters here
12%
of US adults had proficient health literacy
The documents you own
| Document | What it touches |
|---|---|
| Plain-language and lay summaries | EU Clinical Trials Regulation, Annex V |
| Patient medication information | MLR review |
| Informed consent forms | IRB and ethics review |
What you'd use most
Knowledge base with citations
Suggestions come from your approved sources, each with its citation.
Learn moreMLR review
Every change is tracked with its reason, so medical, legal and regulatory reviewers see what changed and why.
Learn moreProtected terms and approved disclaimers
Product names, safety language and approved disclaimers are kept word for word.
Learn more
Try it on one of your documents
Send a blank template, not a copy with a patient's or member's details.
Questions
Will it shorten our MLR cycle?
We don’t promise a cycle time. It catches clarity issues before review, and the review workload calculator shows what your current rounds cost.
Does it change safety language?
No. Protected terms and approved disclaimers are kept word for word.
