FDA cGMP Regular Batch Regulatory and Safety Compliance Testing of Aerosol Products
Project Description
USA LABORATORY
LONG-TERM TESTING
MULTIPLE TESTS
USA FDA cGMP Pharmaceutical Laboratory needed for regular batch regulatory and safety compliance testing of aerosol products which are filled with breathing oxygen to a 1 litre volume.This includes Impurities testing. Our regular batch is 1-100 aerosol cans.
Project Information
Number:21-01209
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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- Reverse Pharmacology Testing
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- Consistency Testing
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- Congealing Temperature Testing
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- Loss on Drying (under Vacuum) Testing
- Loss on Ignition Testing
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- Mineral Analysis Testing
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- Normality Testing
- Organic Acids Testing
- 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
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- Surfactants Testing
- Talc Testing
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- Total Halides Testing
- Total Reducing Compounds Testing
- Unburned Carbon Testing
- Uncarbonized Constituents Testing
- Unsaponifiable Matter Testing
- UV Absorption Testing
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- Elution Testing
- Agar Diffusion Testing
- Bioburden Testing
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- Total Combined Mold & Yeast (TYMC) Testing
- Total Aerobic Microbial Count (TAMC) Testing
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