Health-related decisions require evidence people can understand and trust.

Understand how search and AI shape confidence in pharmaceutical information.

Patients, caregivers and professionals may use search to understand conditions, products, indications, safety, administration, availability, reputation and questions for a qualified healthcare professional.

Search Intelligence examines whether material information is accurate, appropriately framed, supported, consistent, accessible and responsibly owned.

Publication note

Final sector wording, claims and scope require specialist Pharmaceutical, Regulatory, Medical and Legal approval.

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Decision environment

May involve:

Patients Caregivers Healthcare professionals Pharmacies Distributors Publishers Support organisations AI systems Regulated owned content

Not every search reflects purchase intent. It may be educational, clinical, safety-related, access-related or emotionally sensitive.

The first governance requirement is correct classification of
Audience Purpose Evidence Permitted claims Required review
Core information questions
What is this product or treatment?
What is it indicated for?
What should be discussed with a healthcare professional?
What evidence supports the information?
Is the source current?
Is AI accurate?
Are limitations or safety information missing?
Is the content for patients, caregivers or professionals?
Where is the authoritative source?

SI does not provide medical advice.

The evidence customers need to trust →
Exposures
Product-Information Integrity

Approved facts and consistency.

Indication and Audience Integrity

Appropriate content for the intended audience.

Source-of-Truth Governance

Ownership, versioning and approval.

AI Narrative Integrity

Omission, distortion or oversimplification.

Technical Integrity

Accessibility, indexability and presentation.

Reputation and Misinformation

Outdated or unsupported narratives.

Third-Party Representation

Publishers, pharmacies, distributors and other sources.

Evidence and Approval

Claims traceable to approved evidence.

Governing boundary
SI may identify
Inconsistency Omission Distortion Outdated sources Accessibility Source patterns Representation risk Ownership gaps
Search Governance may route to
Medical Regulatory Legal Pharmacovigilance Product Corporate Affairs Digital Information Governance
SI does not determine
Clinical suitability
Treatment
Safety conclusions
Regulatory approval
Medical advice
Exposure and decision effects
Information becomes available
The person evaluates it
An interpretation forms
Confidence or concern changes
A later health-related decision may occur
Distinguish
Observed exposure Observed or inferred encounter Inferred decision effect Validated evidence Unknowns
Possible assessment areas
Source mapping AI capture Omission and distortion Technical accessibility Third-party review Publisher and pharmacy representation Claim traceability Reputation and misinformation Ownership and approval Retention Correction and re-testing
Potential outputs
Pharmaceutical Search Exposure Map Source-of-Truth Register AI Narrative Integrity Record Omission and Distortion Register Approved Claims Traceability Map Technical Integrity Findings Third-Party Representation Review Search Risk Register Governance RACI Evidence and Approval Trail Executive Findings Session
Possible owners
ExposurePossible owners
Product informationMedical, Regulatory, Product
Claims and evidenceMedical, Regulatory, Legal
Patient contentMedical, Regulatory, Communications
AI representationDigital, Medical, Regulatory
Technical accessibilityDigital, IT, Development
Third-party representationCorporate Affairs, Regulatory, Legal
Safety informationPharmacovigilance, Medical, Regulatory
Source controlsInformation Governance, Product, Regulatory
MisinformationCorporate Affairs, Medical, Legal

Final ownership is organisation-specific.

Suitable conditions
AI representation is materially relevant
Product information is distributed widely
A launch or update is planned
Outdated content remains visible
Ownership is fragmented
Technical conditions affect approved information
Third-party representation requires review
A regulated source-of-truth model is needed
What it is not
Medical advice
Regulatory approval
Pharmacovigilance assessment
Clinical evidence review
Promotional approval
Replacement for Medical, Regulatory or Legal
Control over AI or search platforms

Begin with an approved scope and the right sector authorities in the room.

Need a different scope?
Need a group-wide operating model? Explore Enterprise.
Need a focused growth scope? Explore Corporate.
Need a practical owner-led plan? Explore SME where relevant.
Related solutions
Explore FMCG → Explore Enterprise →