Medical Review Process

Last updated: May 10, 2026.

Step 1 — Topic scoping

A clinical editor scopes the page against current NAMS, ACOG, Endocrine Society, and FDA guidance to define the questions a patient is most likely to ask, the conditions and medications involved, and the safety information that must appear.

Step 2 — Drafting against primary sources

Drafts are written using primary sources only — peer-reviewed journals, society position statements, FDA labels, and federal health agencies. Every clinical claim is footnoted to a specific source. AI tools may assist with drafting and editing; AI never produces the final clinical claim unaided.

Step 3 — Fact-check

A second reviewer checks each citation against its source, verifies that statistics match the cited study, and confirms that off-label, compounded, or higher-risk treatments carry the appropriate disclosure.

Step 4 — Physician sign-off

Dr. Ana Lisa Carr, MD, MBA — Board-Certified Family Medicine, NPI 1689841744 — reviews the final page, signs off, and the page is stamped with her name, credentials, and the review date.

Step 5 — Scheduled re-review

Every clinical page is re-reviewed at least every 12 months, or sooner if a major society guideline changes, an FDA action affects a referenced medication, or a reader reports a factual issue via editorial@kindr.health.

What review does not cover

Medical review verifies general accuracy for a patient audience. It is not personalized medical advice. Treatment decisions require a clinician who has reviewed your individual history, medications, and lab results.