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REPORT AN ISSUE

Found a factual, citation, product, regulatory or data issue? Review the correction process and submit the supporting source.

Accuracy and Accountability

GLP1Scientist Corrections Policy

How GLP1Scientist receives, assesses, prioritizes and publishes factual, citation, regulatory and data corrections.

Illustration representing evidence comparison and correction review

What may be reported

Corrections can cover facts, sources, data and presentation

Factual and citation issues

Incorrect statements, inaccurate citations, broken source links or misleading wording.

Regulatory and medicine issues

Outdated approvals, warnings, formulation details or product status.

Trial, patent and company issues

Incorrect clinical-trial, patent, ownership or company information.

Market and access issues

Outdated pricing, availability, market or access data.

Commercial transparency

Undisclosed commercial relationships or misleading paid placement.

Presentation and accessibility

Image, table, formatting or accessibility errors that affect usability or meaning.

Correction process

How a report is assessed

1. Record and locate

The affected URL, statement, table, image or section and supporting information are recorded.

2. Review the source

The original source and the precise context of the published claim are checked.

3. Check current evidence

Newer regulator, study, registry, company, patent or market sources are reviewed where relevant.

4. Classify and act

The issue is classified as an error, update, evolving evidence, interpretive disagreement, formatting issue or unsupported report.

Materiality

Minor, substantive and critical issues

Minor

Spelling, formatting, punctuation or non-substantive wording that does not change meaning.

Substantive

Incorrect facts, misleading comparisons, wrong approval status, inaccurate study results or materially outdated data.

Critical

Information capable of creating serious medical misunderstanding, false safety information, fabricated evidence or materially false regulatory status.

Priority rule: Critical issues receive priority. Submission does not guarantee that the requested change will be made; decisions depend on evidence, source quality, jurisdiction and material effect.