Ten years ago, an analytical testing lab called ChRi Laboratories was born in Saint Paul, Minnesota, to partner with the pharmaceutical, dietary supplements, and hemp industries. Over the years, we have built a customer-centric reputation, which aligns with our ability to be adaptable, streamlined, and productive. Combining a robust internal quality system with an ISO 17025 accreditation sheds confidence with our clients that quality will never be compromised. As a full-service cGMP and FDA Registered laboratory, we focus on helping our clients develop a core understanding of the regulatory requirements related to their specific niche. Upon competition, ChRi provides comprehensive data packages to help you understand your drug substance or product. ChRi Laboratories has extensive experience in the development and validation of various GMP QC test packages for pharmaceutical drug substances, drug products, excipients, and other manufacturing controls. We also possess the expertise to detect, identify, and measure trace amounts of related substances, impurities, and other chemicals in products and materials down to ppm levels. Since our inception, we continue to focus on bridging scientific expertise with innovation to move analytical concepts through the drug development process. By investing in our client’s goals and visions, we form meaningful, lasting relationships that allow us to continue to collaborate.