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Honeyman Group
| Analytical Services |
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From our
audited and approved laboratories we provide
comprehensive chemical, microbiological and
endotoxin testing services supporting a broad range of pharmaceutical
processes and applications including quality critical utilities (water and
steam), sterilisation, cleaning validation, environmental, raw materials and
finished products.
Unlike many standard contract
testing laboratories, Honeyman have the ability to support clients in trend
analysis, interpreting data and in advising on any remedial plant
actions necessary to improve performance or address compliance issues. |
Our Analytical Services Laboratory was
established initially to provide analytical support for high
purity water systems and sterilisation processes by testing
samples necessary for the qualification and routine
monitoring of these specialised facilities.
An on-going contract analysis service is now offered for
these and many other pharmaceutical and related activities
by our testing laboratory.
Our facilities are audited by more than 20 client audit
teams per year. We welcome these client audits as it allows
us to continually monitor and improve our operations. In
addition, our latest successful MHRA audit took place in
August 2006.
Download a copy of the MHRA approval
letter [178Kb]
Drawing upon the extensive industry experience of our
Engineers, and Validation Professionals, Honeyman can offer
clients support and guidance on the collated analytical
data, relating this to their pharmaceutical processes, to
ensure continued compliance assurance is maintained.
Troubleshooting support is also available in the case of
'Out Of Specification' data or process problem
identification and rectification. |
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Chemical Analysis of
Pharmaceutical Samples
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Pharmaceutical Water
Analysis/Sampling, Encompassing Raw Water to Purified Water, Highly
Purified Water and Water for Injection as Defined in the European (EP/PhEur),
United States (USP) and Japanese (JP) Pharmacopoeias
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Washer Disinfector
Water to HTM 2030 Standards
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Clean Steam
Testing to HTM 2031 Standards
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Cleaning
Validation Samples by TOC (Total Organic Carbon) Analysis
Microbiological Testing of Pharmaceutical Samples
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D and Z Value Analysis of Biological Indicators for
Independent Verification
Using our BIER Vessel
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Bio Burden on Cleaning Validation
Samples
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Environmental Bio Burden
Monitoring using Contact Plates, Settle Plates and Air Strips
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Microbiological Bio Burden on
Components (Raw and Packaging Materials)
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API Methods for Microbiological Identification supporting Bio Burden Testing
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Fungal Identification
Specific
Analysis Includes the Following:
Our sampling and transport procedures are validated for
samples taken within or outside of the U.K. We offer clients
an on-site sampling service backed up by collection either
by our own transport or by courier.
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