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Accredited by the College of American Pathologists (CAP) and certified under CLIA for diagnostic and esoteric testing.
Compliant with FDA and ISO standards for molecular diagnostics and custom assay development.
Accreditations:
Certified by CLIA and CAP, with ISO 15189 accreditation through A2LA, emphasizing quality and proficiency across all 50 states, including approvals in New York and California.
Visit Quantigen.com for a full list of accreditations and certifications.
Accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP) for ethical and regulatory review processes.
Visit PearlIRB.com for full list of accreditations and licenses.
Operates under FDA and OHRP guidelines, with a legacy of trust in human subject research protections.
Salus IRB is appropriately constituted, organized, and conducts ethical review in accordance with the U.S. Food and Drug Administration 21 CFR Parts 50 and 56, the Department of Health and Human Services 45 CFR Part 46, and the International Conference on Harmonization (ICH) Guideline for Good Clinical Practice E6(R2).
Salus IRB is registered with the United States Department of Health and Human Services (DHHS) IRB Registration System for OHRP and FDA under parent organization number IORG0005674 and registration numbers IRB00006833 (Board 1), IRB00006834 (Board 2), IRB00009473 (Board 3), IRB00013027 (Board 4), and IRB00013544 (Board 5).
Salus IRB has been fully accredited since 2009 by the Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP).
Expertise in FDA and international regulatory requirements, recognized for its high standards in clinical development services.
Visit PearlPathways.com for all accreditations and certifications.
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