Case Study  ·  Regulatory Intelligence

Tracking a shift in rodent model use.

A global leader in genetically engineered rodent models wanted to know how 2022 guideline changes affected carcinogenicity testing. We analyzed drug approval records with AI and consulted experts to show how transgenic model use changed.

The Client

The client is a global leader in genetically engineered rodent models and services. It wanted to see how new guidance changed model selection for small molecule drug testing.

The Challenge

New guidance.
What really changed?

Prescouter was asked to assess how 2022 carcinogenicity guideline changes affected testing of small molecule drugs and the choice of rodent models, especially transgenic mouse models.

  • Rules

    Guideline change

    International guidance updated in 2022.

  • Models

    Model selection

    Which rodent models were chosen.

  • Market

    Indication trends

    Disease areas favoring transgenics.

Our Approach

Pairing AI-driven record analysis with expert insight.

AI analysis
200+drug approval records

Structure the records

An AI language model extracted drugs, indications and test models from US and EU approvals.

Before and after
2022guideline update analyzed

Compare the eras

We compared carcinogenicity testing before and after the guideline change to spot shifts.

Expert interviews
4experts interviewed

Add the context

Regulatory consultants and pharma toxicologists put the record analysis in context.

The Outcome

Clear signals for a marketing strategy.

Prescouter presented the changes observed after the guideline update, especially in transgenic rodent use. It identified opportunities by indication, since some disease areas were more likely to use transgenic models, and its expert insights helped the client shape a marketing strategy.

  • Shifts

    Post-2022 changes

    Transgenic rodent use tracked.

  • Targets

    Indication opportunities

    Disease areas most likely to adopt.

  • Strategy

    Marketing plan input

    Shaped by expert consultations.

Regulatory changes ripple slowly through drug approvals. Structured data shows the real shift before the market fully notices.

Let’s Talk

How will new rules reshape your market?

Turn regulatory records into a clear view of demand. Wherever you’re starting from, we’ll help you get there.

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