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Contract
Laboratory Services (CLS)
> Pharmaceutical
Analysis >> Cleaning Validation
CLL provides analytical support to your cleaning validation
projects
Cleaning Validation can be used to test for manufacturing
residues, disinfectant and disinfectant metabolites, chemicals,
solvents, by-products, degradants, and
microbial contaminants. CLL provides analytical support to your
cleaning validation projects through on-site project specific teams, as
well as laboratory analysis of samples collected.
Surface
Sampling or Rinse Solutions methods maybe used depending on the
equipment / process.
TOC is one of
the parameters used to detect contamination post-cleaning/disinfecting
activity. Total Organic Carbon (TOC) Analysis is a rapid & reliable
way to check efficacy of cleaning validation projects. Apart from TOC,
we also analyze samples on LC-MS/MS or GC-MS for Cleaning Agent /
Disinfectant / Manufacturing Residues.
Our cleaning
validation report will inform you of the effectiveness of the cleaning
procedure.
INTEGRATED DISINFECTANT VALIDATION
A pre-cursor
to Cleaning Validation is the Disinfectant Validation. Using the
Challenge Method or the Dilution Method, we can ascertain pre- &
post- application bio-loads. Various standard methods from AOAC, USP,
and BP are available to check for the efficacy of Disinfectant
Validation. CLL’s integrated team provides a
smooth change-over from Disinfectant Validation to Cleaning Validation.
For more information on TOC, click here.
To request for more information on Cleaning
Validation, contact us at
info@choksilab.com
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