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Temperature & Humidity Monitoring Log

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What this document is for

Record entries in indelible ink. Each completed step requires initials and date. Cross out errors with a single line, initial and date. Do not obscure original entries.

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Document typeCode
FormFRM-QMS-039

Grounded in

FDA 21 CFR 210/211 and Part 11, EU GMP (EudraLex Volume 4, including Annex 1 and Annex 11), ICH Q7–Q12, and WHO GMP. Supplied in 13 languages.

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