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Make the next claim worth making.

A medicines product earns confidence through useful comparisons. A compelling interface or faster first draft is a starting point; the complete task still has to work for the people responsible for it.

Our planned PHARMORIS evidence cases examine review quality, implementation, appropriate trust and economic value. Each begins with a defined setting and competent existing practice. The purpose is to discover where the approach helps, what it costs to use and which changes would make it better.

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The comparison starts with good existing work

A weak baseline can make an ordinary improvement look impressive. The existing approach deserves to be described fairly: who performs the task, which sources they use, how they check it and what happens when information conflicts.

Agree the outcome before examining a result. A pharmacy group may value dependable follow-through; a medicines committee may need a review that survives professional challenge. The comparison should reflect that purpose and include the effort introduced by a different workflow. Study design and necessary approvals are agreed before evaluation begins.

Evidence-review effort means the whole review

Our first proposed track asks whether assistance makes an evidence task more useful after checking and correction are included. The initial answer may be fluent while omitting a material source or overlooking a local requirement. Finding and repairing that omission takes professional time.

An informative comparison would examine source accuracy, relevance, completeness, critical omissions and total reviewer effort. Qualified reviewers need a consistent basis for judging the work. Speed and quality should be examined together so that the result describes a better review rather than merely a faster beginning.

Follow-through has to be observed

A second track concerns the work after agreement. A decision can be recorded while training, a handover or a supply question remains unresolved. Counting approved proposals alone would miss the operational issue.

We want to examine how a defined change moves through a real process: ownership, completion, delays, queries, rework and support. The comparison needs records that suit the task. It should distinguish an action completed in a tool from a change observed in practice, and account for other events that could explain the result.

Examine appropriate trust

Professional judgement is part of the product question. Can a reviewer recognise a missing source or an unsupported inference? Does the presentation encourage challenge? Does uncertainty help someone identify the next question, or become another detail to ignore?

Planned human-factors work would examine error detection, over-reliance, understanding of uncertainty, workload and accessibility. Different experience levels and working conditions may affect the result. The purpose is to learn which design choices support careful use and where the interface needs to change before the approach can progress.

A useful comparison. A finding worth knowing.

Evidence should help a team decide what to do next.

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The decision before the pilot

What would have
to change?

Give the evaluation a number worth testing.

Explore the relationship between task time, uptake and delivery cost. Your inputs stay in this page. The results describe an assumption, rather than a measured PHARMORIS benefit or a quotation.

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A useful starting point

Start with
your process.

Complete the seven inputs or load the invented example to see the comparison.

Time released can create capacity without reducing a budget. Service quality, safety, access, staff experience and any displaced work need their own evaluation. This one-year comparison excludes discounting, tax, financing and wider effects; it is not a full business case.

Inspect the calculation and the next evidence question

Cases using the approach = relevant cases × uptake ÷ 100. Hours = cases using the approach × (current complete time − proposed complete time) ÷ 60. Staff-time cost equivalent = hours × loaded hourly cost. First-year delivery cost = annual ongoing cost + implementation cost.

Threshold minutes = first-year delivery cost × 60 ÷ (cases using the approach × loaded hourly cost). A negative time difference remains negative. The model does not assume the proposed process is faster.

A useful study would measure complete work in comparable cases, test quality separately and capture training, correction and support. Choose the minimum worthwhile change before collecting results. Distinguishing cash effects from other valued benefits is consistent with HM Treasury | The Green Book (2026).

Count the economics of using the approach

A useful result has to include the work of introducing and sustaining a change. Onboarding, source checking, training, support and local coordination can affect whether the benefit is worth pursuing.

The planned value track separates modelled opportunity from observed resource use and financial effects. Capacity released is different from a cash-releasing saving; a change in expenditure does not automatically establish improved outcomes. A buyer should be able to understand the comparison, the important assumptions and how the result changes when those assumptions are tested.

Let the findings change the programme

A study should be capable of challenging the proposition. The most useful finding may identify a narrower task, a different user group or an approach that adds too much burden. Those results help concentrate development where it can offer greater value.

The NICE evidence standards framework offers relevant context for planning digital-health evidence. The appropriate methods still depend on intended use and the particular question. A clear study should leave participants with an interpretable finding and a justified next decision. These proposed tracks provide a basis for agreeing that work with suitable evaluation partners.

Questions already taking shape.

DMS Commissioner Value Scan is a proposed review of discharge-medicines referral, action and completion gaps. A suitable evaluation would ask whether the resulting account helps commissioners and pharmacy teams identify a worthwhile next action.

A pharmacy-service activation direction would examine readiness, completed consultations, accepted claims and the value remaining after delivery costs. The comparison needs to show whether a service’s apparent momentum is sustained in the actual work.

A hospital outpatient options comparison would examine expected benefit, delivery effort and the conditions needed for an option to work. Hospital and provider economics would be assessed separately, with a defined setting and an agreed comparison before an evaluation proceeds.

Help shape a revealing comparison

We welcome medicines professionals, independent evaluators, researchers and organisations with a defined operational question. A useful contribution might establish the current process, improve the comparison or identify a measure that would genuinely inform adoption.

Tell us the decision the study should support. That allows the discussion to focus on an evaluation with a clear purpose, suitable expertise and a result worth learning from.

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