If you manufacture, import or assess pharmaceutical products, this package supports selected quality-control measurements against an agreed method. For Dissolution Profile Verification, the proposed measurements are Dissolution percentage at sp…
If you manufacture, import or assess pharmaceutical products, this package supports selected quality-control measurements against an agreed method. For Dissolution Profile Verification, the proposed measurements are Dissolution percentage at specified time points under agreed pharmacopeial method. This option is scoped around one submitted sample; any expanded analyte list or duplicate work needs written confirmation. Tell us the sample material, the number of specimens and the reason for testing so we can confirm a suitable analytical method, reporting units and laboratory availability. The price is an estimate; the final scope, methods and laboratory quotation must be agreed before testing begins.
Expanded analyte scope requires a written, validated analyte list and revised quote before sale. The listed base tests are the provisional minimum only. Expanded analyte cost not yet itemised
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