What Is MB Research Laboratories?

Updated

MB Research Laboratories is a contract research organization (CRO) that specializes in toxicology testing and safety assessments for regulated products. According to the company, it has supported pharmaceuticals, medical devices, chemicals, and consumer products with regulatory-ready safety studies for over 50 years. Its work is aimed at companies that need GLP-compliant studies aligned with OECD, EPA, ISO, and DOT standards, particularly for cosmetics, pharmaceuticals, medical devices, chemicals, and consumer products.

What MB Research Does

MB Research provides toxicology and safety assessment services rather than manufacturing or selling products. Its stated focus is generating data that supports regulatory submissions and hazard classification. The company describes its studies as GLP-compliant and aligned with international standards, which matters when results must be accepted by regulators in multiple markets.

The core service areas listed on its site include:

  • Eye and skin safety testing — OECD TG 437, 492, 439, and 431 methods for eye irritation, dermal irritation, and corrosion testing using validated in vitro methods.
  • Biocompatibility testing — ISO 10993 medical device safety, covering cytotoxicity, irritation, and sensitization studies.
  • Acute toxicity testing — an OECD "six-pack" (TG 420, 423, 425, 402, 403) supporting hazard classification and regulatory safety assessments.
  • Skin sensitization testing — OECD TG 442 methods, using in vitro and in vivo approaches to evaluate allergic contact dermatitis potential.
  • Regulatory toxicology testing — GLP-compliant safety studies supporting global regulatory submissions under OECD, EPA, ISO, and DOT standards.

Who It Serves

MB Research organizes its services around five core industries. The table below summarizes what the company says it offers each one.

Industry What MB Research provides
Cosmetics GLP-compliant safety assessments for raw materials, formulas, and finished products; in vitro alternatives such as ocular irritation, dermal irritation, phototoxicity, and corrosivity testing; guidance on global frameworks including the EU Cosmetics Directive (76/768/EEC)
Consumer products End-to-end acute toxicology and safety assessment, including oral, dermal, and inhalation exposure studies, to help meet CPSC, EPA, and international requirements
Pharmaceuticals GLP toxicology testing for regulatory safety assessments
Medical devices Biocompatibility testing under ISO 10993
Chemicals Regulatory toxicology testing supporting hazard classification and submissions

Why the Standards Matter

The value of a CRO like MB Research depends on whether its studies will be accepted by the regulator reviewing your product. Two labels carry most of that weight:

  • GLP (Good Laboratory Practice) — a quality system for how nonclinical safety studies are planned, performed, monitored, recorded, and reported. Regulators generally expect GLP compliance for studies used in submissions.
  • OECD / ISO test guidelines — standardized methods (for example, OECD TG 492 for eye irritation or ISO 10993 for device biocompatibility) that make results comparable across labs and jurisdictions.

If your product needs to clear more than one market, matching the study to the relevant guideline is usually the deciding factor in choosing a lab.

When to Consider MB Research

MB Research is a reasonable fit if you need:

  • GLP-compliant toxicology data for a regulatory submission or hazard classification.
  • In vitro alternatives for eye, skin, or sensitization endpoints, especially for cosmetics where animal testing is restricted.
  • Biocompatibility testing for a medical device under ISO 10993.
  • Acute toxicity studies across multiple exposure routes.

It is likely not the right fit if you need clinical trials, manufacturing, or non-toxicology analytical work, since the site describes a toxicology and safety assessment focus.

Practical Next Step

The site offers a "Get a quote" path and "Learn More" pages for each assay type. To get a useful response, come prepared with your product type, the target market(s), the endpoint(s) you need tested, and any guideline the regulator has specified. Pricing is not published on the page, so cost and turnaround need to be confirmed directly with the lab.