Product Safety Testing

MB Research Laboratories conducts acute, subchronic, chronic toxicology and pharmacology studies. Standard studies at MB are available to meet the product safety testing requirements of the applicable regulatory agencies, or tailored to meet the specific need.

Acute studies are selected and conducted based on the intended use of the test substance and applicable regulatory requirements. Commonly requested protocols, such as below are available upon request.

In Vivo Toxicology Testing (FDA, EPA, OECD, OPPTS)
- Acute EPA and OECD Toxicology Testing
- Dermal Irritation and Contact Sensitization Studies
- Oral and Inhalation Studies
- Subchronic & Chronic Toxicology Testing
- Mucosal Irritation Studies

Subchronic and chronic toxicology studies are conducted at MB Research and are individually designed for the sponsor in order to comply with specific regulatory requirements and intended use of the test substance.

Studies are performed by highly trained and qualified personnel and closely supervised by a Senior Toxicologist at every phase. 

Pathological requirements related to studies are under the direction of a Board Certified Veterinary Pathologist.

For more information regarding MB Research Labs and our capabilities, please download our Capabilities Statement or call a Client Services Agent at 1(215) 536-4110.

Oral, Ocular, Acute Dermal, Dermal Sensitization, Dermal Irritation, Inhalation.

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