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FAQ > Glossary of Terms > A Series > Audit Comment
 

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Pharmaceutical & Cleanroom Glossary of Terms

A Series , B Series , C Series , D Series , E Series , F Series , G Series , H Series , I Series , K Series , L Series , M Series , N Series , O Series , P Series , Q Series , R Series , S Series , T Series , U Series , V Series , W Series , X Series , Y Series , Z Series

First 1 - 35 Words , Next 36 - 70 Words, Analytical Data Interchange (ANDI), Analytical Method, Ancillary Material, Anemometer, Angstrom, Anion, Anoion Exchange Resin, Anneal, Annealing, Antibiotic, Antibody, Antigen, Anti-interferon, Antiseptic, Antiserum, Antistatic, Antistatic Cleaners, Antitoxin, API ( Active Pharmaceutical Ingredient), API(Active Pharmaceutical Ingredient) Starting Material, Apoenzyme, Aquifer, Asbuilt Cleanroom, Ascomycetes, Asepsis, Aseptic, Aseptic Processing, Aseptic Processing Area, Aseptic Transfer (Isolater), ASME Bioprocessing Equipment, Assay, Assimilation, Atomic Absorption Spectrophotometry, Atrest Cleanroom, Audit Comment, Audit Trial, Austenite, Autegoneous Weld, Auto Clave, Auto Immune Disease, Automated System, Automatic Welding, Autoradiography, Autosome, Autotrophs

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Audit Comment
A feature of the audit trail that aids both originator and reviewer in understanding why the originator performed a specific action. CFR 21 Part 11 does not require entering the reason for a record change, but some predicate rules (such as GLPs) do expect an explanation. It is important that the user interface for entering audit comments prevents users from changing the audit trail itself