Roadmap.

Here you can see what we are building now, what we have decided to build next and what we are still considering. When a feature ships, it leaves this page and is described where it belongs.

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Now

Being built now.

  1. Reports in German, French and Spanish

    The same report, on your own template, in each of these languages too.

    Report Template

  2. Last-batch date and retention countdown

    Enter the date the last batch went on the market, and the file shows how much longer the law says you must keep it.

    PIF Files

  3. Document expiry dates

    Add an expiry date to supplier documents and get a reminder before it passes.

    Ingredient Documents

Planned

Decided, not started yet.

  1. File transfer

    When the Responsible Person changes, move a product’s whole file to another company account. The record of who held it is kept.

    PIF Files Audit Log

  2. Variants

    Where the law allows, variants of one product share one file and one report, and count as one product.

    Product List

  3. Inspector view

    A link made for a competent authority: the whole file, including the MoS and toxicology values that a normal share link hides.

    PIF Files Audit Log

  4. Formula versions

    See two versions of a formula side by side, each with the report it produced.

    Product List

  5. GMP record

    One record per manufacturing site with its GMP certificate and expiry date, shown in the Command Center.

    Command Center

  6. Shared blend library

    Common supplier blends, already broken down into their ingredients and provided by the platform. Your own Custom Mix stays private to you.

    Custom Mix

  7. Draft review

    Before the assessor opens it, the CPSR draft gets a second read: gaps, inconsistencies and missing sources are flagged, each with the section it concerns. The assessment stays with the assessor.

    Product ListAI-assisted

  8. API

    Access your products, files and findings from your own systems.

    Platform

Exploring

Being considered, not decided.

  1. Ask your file

    Ask a question about a product’s file and get an answer that names the document it comes from.

    PIF FilesAI-assisted

  2. Suggested toxicology sources

    For an ingredient that isn’t in your library, suggested NOAEL sources with references. Nothing goes into a report until it has been reviewed.

    Toxicology DataAI-assisted

  3. Exposure scenarios

    Total exposure across routes, for products that the SCCS default values don’t cover.

    Product List

  4. Report verification

    A page where anyone with a report’s code can check that it is the report that was signed.

    Audit Log

  5. More markets in Regulatory Watch

    Annexes from markets beyond the EU and the UK, matched to your formulas the same way.

    Regulatory Watch

Common questions

Do you give dates?

No. The three lists show an order, not a calendar. When something ships, it leaves this page and is described on the page it belongs to.

Is anything on this page included in my plan?

Not until it ships and the Pricing page lists it. Nothing here is promised as part of any plan.

How do I suggest something?

Write to us from Talk to us and tell us what you would use it for.

Start with a formula you already have.

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