Partnering For Analytical Excellence

Syngene is a trusted partner for pharmaceutical and biotechnology companies seeking precision-driven, regulatory-compliant analytical solutions. Backed by 300+ scientists, we combine deep scientific expertise with robust global quality systems to support programs from early development through commercialization.

Our capabilities are enabled by Asia’s largest ICH stability infrastructure and a 72,000+ sq. ft. network of dedicated analytical and stability laboratories. This scale allows us to execute complex development programs efficiently while maintaining uncompromising standards of data integrity, quality, and compliance.

We are accredited by leading global regulatory authorities, including the USFDA, PMDA, Health Canada, and CDSCO, and operate under internationally recognized ISO standards such as 9001:2015, 14001:2015, 45001:2018, 27001:2013, and 13485:2016.

We provide end-to-end analytical development services for small molecules, large molecules, and animal health products, spanning method development and validation through stability studies and commercial quality control testing. By integrating advanced infrastructure with strong scientific capability, we help accelerate development timelines while ensuring reliability and regulatory confidence at every stage.