SRC develops and manages data generation for new product offerings, Data Call-Ins (DCIs), and amending existing products in the antimicrobial marketplace. We have extensive experience managing timely contract laboratory services with labs in the U.S. and overseas. SRC is available to conduct on-site Good Laboratory Practices (GLP) audits to ensure studies and final reports are acceptable to various agencies. Our firm has established relationships forged over many years with the laboratories whose data is submitted to EPA, FDA, and international bodies. Our team actively participates in standards setting bodies including ASTM, OECD, AOAC, and NSF.

SRC regularly counsels clients on strategic data generation to control laboratory costs. We provide valuable test points to manage decisions regarding claims, formulation development, and labeling regulations. Our consultants create customized data generation strategies, design test methods, and develop protocols to fit your marketing needs. We consistently monitor the changing domestic and international requirements to confirm protocols and final reports will support product registration and desired marketing claims, allowing us to generate one set of data for global registration. Because our consultants include professionals in all areas of data requirements, the entire suite of required testing can be managed through our firm for U.S. and/or international registrations.