Design the dose architecture.
Deterministic, traceable calculations for device-achievable doses, band-specific combination-product tolerances, capacity, and adjacent-dose overlap.
Architecture visualization
9 doses · 1 ordered dose band · 0 fixed dose adjustments
Dose-overlap optimization
First review the Original Dose Design. Then optionally reduce and redistribute doses using one delivered-dose range.
Priority: maximize dose count; keep both endpoints unchanged; then keep minimum unchanged; then keep maximum unchanged; finally move both by the smallest permitted percentages. Multiple dose bands are optimized as one continuous system. Intermediate band maxima stay fixed as rule thresholds: an Actual Dose at or below a threshold uses the lower band, while a dose above it uses the higher band. Every dose and interface pair is therefore calculated with its applicable band's concentration, increment, device, drug, and ISO parameters. The minimum permitted optimized spacing is measured from the smallest adjacent Actual-Dose gap across the complete Original Dose Design, including band interfaces; a single percentage design uses its smallest original Actual-Dose percentage gap.
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All doses · Desired and Actual values, both scenarios, and adjacent dose variation overlap
Interface limit is governed by the higher band| DOSE | DESIRED DOSE | ACTUAL DOSE | VOLUME | DESIRED INCREMENT | RELEASE RANGE | EOSL RANGE | OVERLAP / SEVERITY | STATE |
|---|---|---|---|---|---|---|---|---|
| B1D1 | 6.00 µg | 6.00 µg | 20.00 µL | — | 4.41 µg–7.65 µg | 4.32 µg–7.80 µg | — | Calculated |
| B1D2 | 9.00 µg | 9.00 µg | 30.00 µL | 3.00 µg · 50.0% | 7.35 µg–10.71 µg | 7.20 µg–10.92 µg | 0.30 µg · 10.0%R 0.30 µg · E 0.60 µg | Review |
| B1D3 | 12.00 µg | 12.00 µg | 40.00 µL | 3.00 µg · 33.3% | 10.29 µg–13.77 µg | 10.08 µg–14.04 µg | 0.42 µg · 14.0%R 0.42 µg · E 0.84 µg | Review |
| B1D4 | 15.00 µg | 15.00 µg | 50.00 µL | 3.00 µg · 25.0% | 13.23 µg–16.83 µg | 12.96 µg–17.16 µg | 0.54 µg · 18.0%R 0.54 µg · E 1.08 µg | Review |
| B1D5 | 18.00 µg | 18.00 µg | 60.00 µL | 3.00 µg · 20.0% | 16.17 µg–19.89 µg | 15.84 µg–20.28 µg | 0.66 µg · 22.0%R 0.66 µg · E 1.32 µg | Review |
| B1D6 | 21.00 µg | 21.00 µg | 70.00 µL | 3.00 µg · 16.7% | 19.11 µg–22.95 µg | 18.72 µg–23.40 µg | 0.78 µg · 26.0%R 0.78 µg · E 1.56 µg | Review |
| B1D7 | 24.00 µg | 24.00 µg | 80.00 µL | 3.00 µg · 14.3% | 22.05 µg–26.01 µg | 21.60 µg–26.52 µg | 0.90 µg · 30.0%R 0.90 µg · E 1.80 µg | Review |
| B1D8 | 27.00 µg | 27.00 µg | 90.00 µL | 3.00 µg · 12.5% | 24.99 µg–29.07 µg | 24.48 µg–29.64 µg | 1.02 µg · 34.0%R 1.02 µg · E 2.04 µg | Review |
| B1D9 | 30.00 µg | 30.00 µg | 100.00 µL | 3.00 µg · 11.1% | 27.93 µg–32.13 µg | 27.36 µg–32.76 µg | 1.14 µg · 38.0%R 1.14 µg · E 2.28 µg | Review |
Transparent calculation chain
ISO 11608-1 is treated as a minimum boundary. Better performance is allowed; worse performance is visibly flagged. This screening tool does not make a regulatory compliance determination.
Save and compare up to three systems
History includes all dose bands, parameters, detached states, Actual Doses, Release/EoSL maxima, capacity, and ISO status.
DAD-PROTOTYPE-01
Generated 11/6/2026, 9:49:37 PM · 1 dose band(s) · Governing scenario: End of shelf life
Calculated dose table
| Dose | Desired Dose | Actual Dose | Volume | Release range | EoSL range |
|---|---|---|---|---|---|
| B1 · D1 | 6.00 µg | 6.00 µg | 20.00 µL | 4.41–7.65 µg | 4.32–7.80 µg |
| B1 · D2 | 9.00 µg | 9.00 µg | 30.00 µL | 7.35–10.71 µg | 7.20–10.92 µg |
| B1 · D3 | 12.00 µg | 12.00 µg | 40.00 µL | 10.29–13.77 µg | 10.08–14.04 µg |
| B1 · D4 | 15.00 µg | 15.00 µg | 50.00 µL | 13.23–16.83 µg | 12.96–17.16 µg |
| B1 · D5 | 18.00 µg | 18.00 µg | 60.00 µL | 16.17–19.89 µg | 15.84–20.28 µg |
| B1 · D6 | 21.00 µg | 21.00 µg | 70.00 µL | 19.11–22.95 µg | 18.72–23.40 µg |
| B1 · D7 | 24.00 µg | 24.00 µg | 80.00 µL | 22.05–26.01 µg | 21.60–26.52 µg |
| B1 · D8 | 27.00 µg | 27.00 µg | 90.00 µL | 24.99–29.07 µg | 24.48–29.64 µg |
| B1 · D9 | 30.00 µg | 30.00 µg | 100.00 µL | 27.93–32.13 µg | 27.36–32.76 µg |
Formulas and warnings
Overlap width = MAX(0, MIN(upper A, upper B) − MAX(lower A, lower B)); overlap percentage = overlap width ÷ (Actual Dose B − Actual Dose A) × 100, or “-” when Actual Doses are equal. Band 1: complete the last-dose accuracy assessment required for variable-dose A/C systems. Band 1: an absolute device tolerance exceeds 5% of a dose volume below PT. Band 1: residual/dead volume is zero; confirm it is measured or justified. Band 1: engineering reserve is zero; confirm that no reserve is required. Band 1: Residual / dead volume starts at zero; define a non-zero absolute minimum/maximum range before allowing optimization. Band 1: Engineering reserve starts at zero; define a non-zero absolute minimum/maximum range before allowing optimization. Band 1: Maximum dose variation overlap starts at zero; define a non-zero absolute minimum/maximum range before allowing optimization. At least one Release adjacent-range intersection exceeds the maximum overlap limit of its governing higher band. At least one End-of-shelf-life adjacent-range intersection exceeds the maximum overlap limit of its governing higher band.