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The specificity of the Fluorescence microscopic immunohistochemical procedures was validated by omitting the primary antibodies or by using nonimmune serum instead of the primary antibodies.
Equipment used in these procedures was validated to ensure proper installation, operation, and performance.
Completeness of entered procedures was validated in 2 ways: (1) by comparison with the number of reimbursements for arthroplasty surgeries (Vektis database), and (2) by comparison with data from hospital information systems (HISs).
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In conclusion, the proposed analytical procedures were validated over the selected validation domains for fruit juices and came out on very capable techniques.
The analytical procedures were validated according to the ICH guidelines for validation.
The cleanup procedures were validated to maximize recovery yields of the analytes, and to minimize procedural blank and interference with GC/MS measurements caused by residual contaminants.
The estimation procedures are validated with extensive laboratory measurements.
Both procedures were validated according to the ICH and FDA guidelines.
The proposed design procedures were validated using the experimental test data available in the literature.
The modelling procedures were validated firstly through comparison with existing test data and secondly through the testing and analysis of representative structures.
Procedures were validated by mass spectrometry (MS) methods.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com