Certified Laboratories, Inc. is a fully validated, FDA compliant cGMP pharmaceutical testing facility.
In addition to the broad spectrum of analyses we currently offer to the consumer products industry we also provide a wide array of USP, CTFA and AOAC and American Water Works Association methodologies to ensure the quality of the pharmaceuticals, cosmetics and nutritional supplements you manufacture. Whether you are undergoing validation projects which require repetitive sampling, need an outside facility for batch release testing or raw material analysis; Certified Laboratories, Inc. , has the analysts and systems in place to perform among others:
Microbiological Analyses
Preparatory Testing for Microbial Limits Test (MLT) USP 61 NF2021
- Full Microbial Limits (MLT) Analysis USP 61 NF 2021 or choose individual requirements:
- Total Aerobic Plate Count
- Total Yeast and Mold Count
- For E. coli
- For Salmonella spp.
- For Pseudomonas spp.
- For Staphylococcus aureus
- Bioburden Analysis
- Analysis of USP Waters by Membrane Filtration:
- Total Coliform Count
- Total Pseudomonas spp.
- Heterotrophic Plate Count
- Total Staph aureus Count
- Multiple Tube Fermentation (MPN) for Water
- USPAntimicrobial Effectiveness Test
- CTFA Preservative Adequacy Testing
- USP Antibiotic Assay
- USP Vitamin Assay
- Bacteriostasis/Fungistasis Testing
- Sterility Testing Membrane Filtration or Direct Inoculation
- Microbial Identifications:
- Bacterial Isolates
- Yeast Isolates
- Mold Isolates
- Bulk Testing of Validation Samples
Certified Laboratories, Inc. , is staffed 365 days a year. Not only will your samples be processed and tested with the highest degree of accuracy and efficiency, we will provide you with the fastest turnaround time possible.
Moreover, we back our clientele with the support that you demand from your contract testing facility…
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