Pharmaceutical

Accelerating Safety with GLP-Compliant Testing

Unrivaled Expertise in Preclinical Toxicology

Since 1972, MB Research has partnered with pharmaceutical companies and government agencies to advance the safety and efficacy of new medical products. With deep expertise in toxicology, safety evaluation, and regulatory testing, we provide reliable, science-driven support for preclinical development. Our legacy of excellence continues to shape the future of pharmaceutical toxicology—delivering trusted results for industry and government alike.

Rely on our experience in the classification of your fast-moving products using our testing models.

Partnership Built on

Personalized Study Management

At MB Research Labs, every preclinical study matters. As a trusted GLP-compliant contract research organization (CRO), we understand that no two testing programs are alike. Whether you require GLP or non-GLP toxicology testing, our approach is centered on personalized study management — tailored to meet your scientific objectives, regulatory requirements, and timelines.

When you partner with MB Research Labs, you gain:

  • Dedicated Study Directors who provide hands-on oversight and direct communication throughout your project.

  • Seamless cross-functional coordination across our scientific and regulatory teams to ensure precision, efficiency, and compliance.

  • Transparent communication that keeps you informed and confident from study design through final report delivery.

At MB Research, partnership means personalized service, scientific integrity, and results you can trust.

Working with

USP/ISO Standards and the FDA

The United States Pharmacopeia (USP) is a scientific non-profit organization that sets public standards for identity, strength, quality and purity of medicines in the United States. The International Organization for Standardization (ISO) is an international standard development organization composed of representatives from the national standards organizations of member countries. ISO publishes certain standards (ISO 9001, ISO 9001, ISO 14001, ISO 45001, ISO 50001) that help in maintaining the quality, efficiency, and safety of pharmaceutical products. The Food and Drug Administration (FDA) relies on USP and ISO standards as part of its work to ensure the safety and quality of foods and drugs. Visit our Regulatory Testing Page for more information on our assays or call us directly and speak with our Client Services department.