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Validacija analitičke metode

Validacija analitičke metode je sistematičan proces uspostavljanja dokumentovanog dokaza da je analitička metoda pogodna za njenu nameravanu upotrebu u merenju identiteta, čistoće, jačine i/ili sadržaja supstance. Regulisana od strane regulatornih agencija (FDA, ICH) i industrijskih standarda (USP, EP), validacija osigurava da su analitičke metode pouzdane, tačne i pogodne za kontrolu kvaliteta u farmaceutskoj, prehrambenoj, hemijskoj i ekološkoj industriji. Validacija metode je obavezna za regulatorne prijave i predstavlja kamen temeljac dobre proizvođačke prakse (GMP).

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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/sr/analytical-chemistry/method-validation-analytical

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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 sa https://scholargate.app/sr/analytical-chemistry/method-validation-analytical · Skup podataka: https://doi.org/10.5281/zenodo.20539026