Contract Laboratory has received the following Environmental Laboratory Test Requests which need to be fulfilled! These Laboratory Test Requests are received from a variety of sources ranging from start-up companies to large, multinational Fortune 500 corporations, international organizations, well-respected universities and government agencies that are actively seeking Independent, Third-Party Environmental Laboratories to perform their Environmental Testing, Analysis, Assays, Product Development, Scientific Research Experiments, Inspections, Certifications, and Engineering Projects. If you are a Environmental laboratory that would like more information on these Environmental projects, please visit our registration page or call toll us free 1-855-377-6821.
TBT testing: We would like to test water samples from marinas for TBT (Tributyltin) and other Organo-tin levels. We would collect the samples ourselves and send them to you. Please estimate the costs for the toxicology and environmental testing as well as the equipment needed for shipping. We also would like to know, how much TBT tests on sediments would be.
GMP Contract laboratory need for performing standard routine sterility, microbiological and analytical tests according to GMP and local regulation. The microbiological tests will include sterility validation, performing sterility tests routinely and incubating and analyzing results of environmental monitoring. The analytical tests will be general Pharmacopeia related tests using IR, NIRS, HPLC, GC, etc.
European FDA regulated pharmaceutical company of sterile products needs laboratory to perform DNA or RNA typing of microorganisms. To verify the sterility of our product we perform sterility testing on every autoclaved load of the batch.
If we get a sterility fail then all the environmental monitoring plates exposed in the sterility test suite are checked for growth. if the data of the miroboligical monitoring of the sterility testing facility show a fault and a pathway can be documented for ingress of the contaminant to the test culture then the test can be declared invalid and a retest performed. So basically if the same microbe is found on a settle plate in the sterility test facility as in the sterility canister and a pathway can be found whereby the microbe was introduced into the canister(i.e from analyst glove)then a retest can be performed. We use an API to check whether or not the organisms found in the canister and plates are the same.
However this is not acceptable for products for the Australia. They require DNA/RNA molecular typing to prove that the organisms are the same in order for a retest to be performed.
GMP Compliant lab to perform the following: Full Monograph Testing (individual and total) for the following items:·,Magnesium Stearate·,Maltodextin·,Polyethylene Glycol·,Silicon Dioxide,·Stearic Acid·,Croscarmellose Sodium,,Dibasic Calcium Phosphate·,Lactose Monohydrate·, Specific Rotation for Ephedrine HCl·,Diphenhydramine HCl Organic Nitrogenous Bases for a pharmaceutical company
assess the androgenic activity, in a quantitative fashion, of a single steriod with the trivial name tetrahydrogestrinone(THG) in a pilot scale study. Either an aquatic organism model or rodent model would appear adequate to provide the information desired but other potential testing types will be considered such as in-vitro receptor binding studies. The study should compare the relative androgenicity of THG to a reference compound such as testosterone
Bioanalytical Laboratory needed for Vitamin detection on Fetal Bovine Serum. Following is a list of vitamins and detectable units:
Vitamin B-12 pg/mL
Folic Acid ng/mL
Vitamin B-6 ng/mL
Thiamin B-1 ng/mL
Vitamin H Biotin pg/mL
Riboflavin B2 ng/mL
Vitamin A Retinol ng/mL
Vitamin C ng/mL
Microbiology Laboratory needed for microbial analysis SB 3112. The test material consisted of only the bacterial spores at a count of 55 x 107 cfu/ml. The tests were run in compliance with the following protocols: 1 USEPA FIFRA;GLP Standards 40 CFR 160 2 USEPA TSCA 40 CFR 792 3 Org. Economic Coop. and Dev. Principles of GLP, Annex 2, C(97)186 4 Japan Ministry of Ag, Forestry & Fisheries, Notification No. 59 Noshan 3850, Director-General of Agricultural Prod. Bureau, 10 Aug 84
Preclinical toxicology laboratory needed for Cytotoxicity studies: MEM Elution Sample Amount: 120 cm2 or 4 grams Irritation: Intracutaneous Reactivity (ISO) (w/2 extracts) Sample Amount: 240 cm2 or 8 grams Sensitization: Magnusson-Kligman (w/2 extracts) Sample Amount 600 cm2 or 32 grams (6 samples minimum) Sensitization: Local Lymph Node Assay: Sample Amount 400 cm2 or 20 grams