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 intended for comparison of three samples using the confirmed analysis list. 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.
Three separately identified specimens; listed assays apply to each specimen.
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