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At Frontage, our business is built on collaboration with a broad spectrum of clients across the pharmaceutical and biopharmaceutical industry—from top global pharma companies to emerging start-ups. We support innovator, generic, and consumer health organizations with IND, NDA, ANDA, and 505(b)(2) submissions, delivering flexible, customized solutions to meet each client’s unique needs. • Laboratory Services: DMPK and CMC services delivered by more than 400 scientists across three facilities in the US and China. Our senior scientists average 10–15 years of experience in complex drug development, many with backgrounds in leading pharmaceutical companies. • Global Bioanalysis and Central Laboratories: A rapidly expanding platform with operations in the US, China, and Europe (Milan), supporting Phase I–IV clinical trials. Services include large molecule bioanalysis (PK/ADA/NAb), safety and specialty testing, advanced biomarker solutions (soluble, tissue, flow cytometry), and genomics, all under a harmonized quality system (CLIA, CAP, ISO, ICH GCP). With a focus on protocol agility, risk-based compliance, and global logistics, Frontage offers both scientific expertise and operational flexibility, enabling sponsors to accelerate development while ensuring data quality and regulatory confidence. • Clinical Services: Phase I–IIa and biometrics capabilities, including a 160-bed clinical unit in Secaucus, NJ, and 18 clinical sites with over 300 beds in China. Our biometrics services support programs from early to late stage. Our commitment to scientific rigor and regulatory compliance ensures the highest quality outcomes. Over the years, we have successfully advanced hundreds of molecules from early development through commercial launch in global markets. With an integrated portfolio of laboratory and clinical services, Frontage provides comprehensive support across the entire product development pipeline.

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