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Demonstration · Global Compliance · 3 steps

From a new market to an evidenced obligation register

Establish which obligations apply to a planned expansion, check the evidence for them, and see whether you will be ready by the audit date.

Example: Pellam Diagnostics Ltd (fictional) · Head of regulatory affairs. Fictional data and a scripted answer.

What happened
The company plans to sell in a new region and an external audit of its regulatory file is set for ten weeks from now.
The question
Which obligations apply to us there, how good is our evidence for them, and will we be ready in time?

The journey, step by step

Simulation. A scripted journey on fictional data, not produced by a live model. Each step uses what you decided in the steps before it, and only the figures are computed.

  1. Which obligations applyAnswer questions about the plan. Each obligation applies, does not apply, or is undetermined until its questions are answered.Open

    Answer questions about the plan. Each obligation applies, does not apply, or is undetermined until its questions are answered.

    Answer the questions about the organisation. Each rule becomes applicable, not applicable, or undetermined until the questions it depends on are answered: nothing is assumed.

    Questions about the organisation

    Will the company place the device on the market there itself?

    Does the device include software that influences a clinical decision?

    Will patient data be processed in the region?

    ObligationWhereStatusEvidence and owner
    Manufacturer registration
    Synthetic Device Act, s. 4
    Region BUndeterminedNeeds: Will the company place the device on the market there itselfNone needed
    Clinical evaluation of software
    Synthetic Device Act, s. 9
    Region BUndeterminedNeeds: Does the device include software that influences a clinical decisionNone needed
    Patient data localisation
    Synthetic Data Code, art. 12
    Region BUndeterminedNeeds: Will patient data be processed in the regionNone needed
    Distributor due diligence
    Synthetic Device Act, s. 6
    Region BUndeterminedNeeds: Will the company place the device on the market there itselfNone needed
    Applies
    0
    Does not apply
    0
    Undetermined
    4
    Answered
    0 of 3

    0 obligations apply, 0 do not, and 4 are undecided.

    Each depends on facts about the plan [S1]; where a fact is not yet given the obligation is undetermined and nothing is assumed. For those that apply the register names the evidence and owner: 0 evidence items, 0 owners.

    Relies on: S1 · Obligation library, regional extract

    The head of regulatory affairs decides. Approving records the applicable obligations as the basis for the evidence review. It does not file anything.

    Not ready. 4 obligations are undetermined until the questions they depend on are answered. Answer them first; nothing is assumed.

Next: How good is the evidence. It opens when the step above is complete.

Limits of this example

  • Synthetic obligations; a real analysis uses the legal text.
  • A scripted journey: no regulator was contacted.
  • This is a scripted demonstration on fictional data. No model was called and no real organisation, person or result is shown.

The other journeys