The Scoring Rubric

22 criteria. Four dimensions.
Openly published.

This is the full DrQScore rubric. Every point is aligned to the ABPI Code of Practice and assessed independently. You know exactly what we look at, and how each point is awarded, before you submit — because a quality standard is only credible if its method is transparent.

100
points total
4
dimensions
22
scored criteria
24 mo
assessment validity

How the assessment works

Content is assessed against the criteria below by qualified reviewers, independent of the company being scored. The points across all four dimensions sum to a single 0–100 score, which maps to a tier.

Independent & qualified

Assessments are performed by healthcare professionals and regulatory-affairs specialists with ABPI signatory experience, independent of the company assessed.

ABPI Code-aligned

Criteria are derived from the ABPI Code of Practice and established regulatory expectations (SmPC consistency, prescribing information, adverse-event reporting, audience controls).

You cannot pay to improve a score

Scores follow the criteria alone. No company can pay to raise, remove or suppress a score. If you believe a score is incorrect, you may submit a formal appeal with evidence.

Valid for 24 months

Assessments mirror the ABPI Code's two-year review cycle. We send renewal reminders at 20 months; expired scores are greyed out on the badge until renewed.

The score tiers

Your total across the 22 criteria places the content in one of four tiers. Content awaiting assessment shows as Pending.

Platinum

90–100

Gold

75–89

Silver

60–74

Below Standard

under 60

Pending

not yet assessed

The 22 criteria

Grouped into the four dimensions, with the points available for each. Descriptions summarise what a reviewer assesses; the full assessment applies the detailed ABPI Code-aligned checks appropriate to the content type.

🔬

D1 — Evidence & Accuracy

Are the claims true, on-licence, and fairly supported by evidence?
40
points · 7 criteria
RefCriterionPoints
D1.1
On-licence accuracy
Indications, patient groups and lines of therapy are fully consistent with the current UK SmPC, with no implication of off-label use.
7
D1.2
Substantiated efficacy claims
Efficacy claims are accurate, qualified by population, timeframe and comparator, and avoid absolute or guaranteed-outcome language.
6
D1.3
Fair safety representation
Safety and tolerability are balanced; key risks, warnings and major contraindications are reflected and the product is not implied to be risk-free.
6
D1.4
Supported comparative & economic claims
Any comparison or cost claim uses appropriate data, populations and endpoints; no unsupported "best-in-class" or superiority language.
5
D1.5
Traceable referencing
Data claims are supported by identifiable, reasonably current references (study, author, year, journal or data on file) an HCP could locate.
6
D1.6
Transparent study presentation
Study design, population, endpoints and duration are summarised fairly; post-hoc, exploratory and subgroup analyses are clearly labelled.
5
D1.7
Overall balance & non-misleading presentation
Taken as a whole, benefits and risks are reasonably balanced; graphs and visuals are not misleading through scale, truncation or emphasis.
5
👁️

D2 — Transparency & Disclosure

Can the reader see what it is, who made it, and how to report a problem?
25
points · 6 criteria
RefCriterionPoints
D2.1
Clear product identity
Product name, form, strength and the indication(s) discussed are clearly stated, including which strengths or formulations apply.
4
D2.2
Prescribing information accessible
Prescribing information is present as text or via a clearly associated single-click link or QR code that reaches current PI in one step, per the ABPI Code.
5
D2.3
PI consistency & legal particulars
Indications, dosing and safety in the PI are consistent with the body of the material; legal classification and cost are included as required.
4
D2.4
Adverse-event reporting present
The required adverse-event reporting statement (MHRA Yellow Card and company contact) is present, prominent and not truncated or obscured.
5
D2.5
Authorship, funding & interests disclosed
The responsible party, funding/sponsorship and any conflicts of interest are disclosed, so the reader can see who produced the content and why.
4
D2.6
Version & date of preparation
A clear job/reference code and date of preparation identify the current approved version and distinguish it from superseded ones.
3
🎯

D3 — Audience Appropriateness

Is it aimed at, and reaching, the right audience — and nobody it shouldn't?
20
points · 5 criteria
RefCriterionPoints
D3.1
Correct content classification
The material is correctly and consistently classified — promotional, educational or non-promotional — across all its parts.
4
D3.2
Defined, appropriate audience
The intended audience (e.g. specific HCPs vs public/patients) is clear and consistent with the content's language, layout and distribution.
4
D3.3
Adequate access control & gating
Where content is HCP-only, appropriate access controls or gating are in place so the public is not inadvertently exposed to HCP promotion.
4
D3.4
No disguised promotion
Promotional and educational content are not conflated; disease-awareness or educational framing is not used to disguise product promotion.
4
D3.5
Appropriate distribution & channel
The distribution channel suits the audience and won't cause the material to act as advertising of a prescription-only medicine to the public.
4

D4 — Process & Compliance Signals

Does it show the marks of a properly governed, reviewable process?
15
points · 4 criteria
RefCriterionPoints
D4.1
Certifiable / MLR review evident
The material is prepared so it can undergo formal medical signatory certification (MLR) or equivalent approval before use.
4
D4.2
Version control & approval status
A clear version identifier and dating distinguish the current approved version; no draft or superseded content is in use.
4
D4.3
Audit trail withstands scrutiny
Sufficient codes, references and rationale exist for the material to withstand external scrutiny such as a PMCPA case review.
4
D4.4
Data privacy obligations met
Where personal data is collected, GDPR obligations (consent mechanisms, privacy notice) are met and clearly signposted.
3
Why openly published? Other quality schemes keep their methodology private. We don't. Publishing the rubric means the score means the same thing to everyone — the company being assessed, the HCP reading the content, and the patient relying on it.
Note for review: this rubric is derived from your ABPI Code-aligned content-review framework and distilled into the four public dimensions. It resolves the earlier mismatch (the homepage lists 5 / 5 / 4 / 3 = 17 criteria) by keeping your published point weights (40 / 25 / 20 / 15) and distributing 22 criteria as 7 / 6 / 5 / 4. Edit any criterion, and I'll update the homepage counts to match once you approve.

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