Frontage Laboratories

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We are a CRO providing integrated, science-driven, product development services throughout the drug discovery and development process to enable life science companies to achieve their drug development goals. We have enabled many innovator, generic and consumer health companies of all sizes to file IND, NDA, ANDA, BLA and 505(b)(2) submissions in global markets allowing for successful development of important therapies and products for patients. We are committed to providing rigorous scientific expertise to ensure the highest quality and compliance.  We have successfully assisted clients to advance hundreds of molecules through development to commercial launch in global markets.

We benefit greatly from having operations in both the United States and China (the two largest markets for CRO services in the world) and are well placed to capture growth opportunities in both markets. Our “Two Countries, One System” approach is integral to our commitment to high quality standards. This approach assures our customers the same quality standards, operating procedures and systems in both China and the United States, whilst also providing our customers with a detailed and highly experienced understanding of the regulations and requirements for drug discovery and development in both countries. This approach enables us to be a partner of choice for companies with multinational requirements or companies that need support for parallel submissions with the US FDA and China FDA.

Related Resources

Outsourcing Analytical Testing for Biologics - A CRO's Perspective

Outsourcing Analytical Testing for Biologics - A CRO's Perspective

Content provided by Frontage Laboratories

White Paper

Biologics are complex large molecules derived from living organisms or manufactured from cells, and they have inherent structural heterogeneity. Indeed, proteins, given their chemistry, are the “most structurally complex and functionally sophisticated...

How to Avoid Surprises in Small-Molecule Drug Development Programs

How to Avoid Surprises in Small-Molecule Drug Development Programs

Content provided by Frontage Laboratories

White Paper

Over the years, the pharmaceutical industry has made steady progress in improving the safety of drugs in development. Consequently, in 2015, only 14 percent of Phase III studies failed due to safety (compared to 55 percent for efficacy), down from 21...

Validating The Simoa Technology

Validating The Simoa Technology

Content provided by Frontage Laboratories

White Paper

Frontage is the first and only laboratory to validate Quanterix’ Simoa HD1 Analyzer for performing immunoassays. Most of the advanced instruments used in bioanalysis—such as Gas Chromatography (GC), High Performance Liquid Chromatography (HPLC), and...