USP Microbial Limit Testing FDA GMP
Project Description
USA LABORATORY
URGENT
USA FDA GMP Pharmaceutical Microbiology Laboratory needed for USP Microbial Limit testing performed under GMP utilizing the Russian monograph test procedure on anesthesia product. We would need it completed within 6 weeks. We can provide method and copies of USP testing performed of a similar nature. This will be recurring but consider this a one time request at this point.
Project Information
Number:21-00082
Industry:Pharmaceuticals
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Other pharmaceuticals laboratory services.
Other Pharmaceuticals testing, analysis, scientific research and development, inspection, certification, engineering, failure investigation, and product development needs include :
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- Finished Product Quality Control Release Testing
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- Hardness Testing
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- Loss on Drying (under Vacuum) Testing
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- Mineral Analysis Testing
- Non-aqueous Titration Testing
- Normality Testing
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- Organic Extractives Testing
- Oxidizing Substances Testing
- Peroxide Value Testing
- Pour Point Testing
- Reactivity Testing
- Reactivity to Water Testing
- Reducing Substances Testing
- Refractive Index Testing
- Residue on Evaporation Testing
- Residue on Ignition Testing
- Saponification Value Testing
- Sieve Analysis Testing
- Silver Reducing Substances Testing
- Silicon Testing
- Sulfur Testing
- Sodium Testing
- Specific Gravity Testing
- Specific Rotation Testing
- Sugars Testing
- Sulfur Compounds Testing
- Surfactants Testing
- Talc Testing
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- Total Halides Testing
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- Unburned Carbon Testing
- Uncarbonized Constituents Testing
- Unsaponifiable Matter Testing
- UV Absorption Testing
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- Total Combined Mold & Yeast (TYMC) Testing
- Total Aerobic Microbial Count (TAMC) Testing
- Testing
