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Honeyman specialise in the microbiological analysis
and identification of raw materials, finished products and pharmaceutical water
(Purified Water, Highly Purified Water,
Water for Injection) from Raw Feed Water through to Process Water
at Point of Use. |
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Our Microbiological Analysis Services include:
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Total Viable Counts
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Absence of
Specific Organisms
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Identification of
Micro-Organisms
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Bio Burden Analysis - A complete Bio
Burden analysis service to quantify and identify microbial Bio Burden
enabling our clients to demonstrate the effectiveness of control
measures employed during the preparation and handling of components,
equipment and removable machine parts prior to sterilisation.
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Microbial Limit Testing - Whether raw
materials, primary, intermediate or finished products we perform
microbial limit testing in the determination of the number of viable
aerobic micro-organisms and specific microbial species.
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Preservative Efficacy Testing - We test
pharmaceutical products such as multi-dose injections, topical
preparations and oral products using our EP and USP compliant methods.
According
to the requirements of:
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Current European Pharmacopoeia
(EP/PhEur) Monographs for Purified Water,
Highly Purified Water or Water For Injection
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Current United States Pharmacopeia (USP)
Monographs for Purified
Water or Water For Injection
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Specific Client Standards
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EC Directive 98/83/EC
Standards for Drinking Water
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HTM 2030
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