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09 Jul 2024

HPLC Analytical Method Development and Validation 2024

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Liquid chromatography is a common method for analyzing pharmaceuticals to assess purity, impurities, and degradation products. Validation typically concentrates on the methodology and standard operating procedure, but audits also cover instrument validation and related items like columns, solvents, and reagents.

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Timings

09:00 AM-06:00 PM (expected)
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Estimated Turnout

upto 1000
Visitors

20 - 100 Exhibitors Based on previous editions

Event Type

Trade Show

Editions

Jul 2024 Interested
+4 more editions

Frequency Bi-annual

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ComplianceIQ USA1227 Total Events
EditionJul 2024

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