Process / pipelineQuality Assurance and Validation

Validiranje analitičke metode

Validiranje analitičke metode je sustavni proces uspostavljanja dokumentiranih dokaza da je analitička metoda prikladna za svoju namjenu u mjerenju identiteta, čistoće, jačine i/ili sadržaja tvari. Regulirano od strane regulatornih agencija (FDA, ICH) i industrijskih standarda (USP, EP), validacija osigurava da su analitičke metode pouzdane, točne i prikladne za kontrolu kvalitete u farmaceutskoj, prehrambenoj, kemijskoj i ekološkoj industriji. Validiranje metode je obvezno za regulatorne prijave i temelj je dobre proizvodne prakse (GMP).

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Method map

The neighbourhood of related methods — select a node to explore.

Izvori

  1. Food and Drug Administration. (2015). Analytical Procedures and Methods Validation: Chemistry, Manufacturing, and Controls Documentation. FDA Guidance for Industry. link
  2. International Council for Harmonisation. (2005). ICH Q2(R1) Validation of Analytical Procedures: Text and Methodology. ICH Harmonised Tripartite Guideline. link
  3. United States Pharmacopeia. (2021). Chapter <1225> Validation of Compendial Procedures. USP 44-NF 39. link

Kako citirati ovu stranicu

ScholarGate. (2026, June 3). Analytical Method Validation. ScholarGate. https://scholargate.app/hr/analytical-chemistry/method-validation-analytical

Which method?

Set this method beside its closest kin and read them side by side — the library lays the books on the table; the choice is yours.

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ScholarGateAnalytical Method Validation (Analytical Method Validation). Preuzeto 2026-06-15 s https://scholargate.app/hr/analytical-chemistry/method-validation-analytical · Skup podataka: https://doi.org/10.5281/zenodo.20539026