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Contract
Laboratory Services (CLS)
> Pharmaceutical Analysis
>> Residual Solvents Analysis / Organic
Volatile Impurities
From
1
st
July 2007, USP (
United States
Pharmacopoeia) has made it mandatory for Residual Solvents to be
determined in all USP products. CLL is well-geared to assist
industry to meet this requirement.
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PARAMETERS:
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Residual
Solvents (Identification, Quantification, Confirmation)
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INDUSTRY
APPLICATIONS:
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Residual
Solvents in Raw Materials, Formulations, & Excepients.
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Other
industry segments: Dry Powders, Liquids, Suspensions,
Cement, Agrochemicals, Dairy, Food Additives, Cosmetics,
Precious Metals & Stones, Minerals, Toners,
Paints/Pigments etc.
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INSTRUMENTS:
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Perkin
Elmer Clarus 500 (TurboMatrix HS Autosampler with
Headspace / Purge-n-Trap, Detectors: FID / PID / MS
connectivity),
Shimadzu
AOC 2000 (with automated sample preparation)
(6 GC-HS instruments)
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SPECIFICATIONS:
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USP,
BP, IP, EP, JP, CP, Client Specifications
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Click
here for More information on ICH Q3C Guideline on Residual
Solvents.
We
also carry out Residual Solvents / OVIs METHOD DEVELOPMENT &
VALIDATION AS PER ICH guidelines.
To
request for residual solvents analysis, write to us at info@choksilab.com
.
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