Nitrosamine Impurity Testing Services
Syngene’s Center of Excellence for Nitrosamine impurity testing supports formulation requirements for small molecule APIs, key sourcing materials, and intermediates.
ICH Stability services
One of the largest Stability facilities in Asia, Syngene supports both small molecules and biologics from early development to CMC
Clinical Development services
Syngene supports early-phase to late-phase clinical trials required for drug development programs across a wide range of therapeutic areas.
Comprehensive solutions for Clinical Development of generic drugs
Synene has developed more than 100 assays for conducting BA/BE studies across small molecules and biologics.
Commercial Manufacturing services
Syngene supports manufacturing of regulatory starting materials, APIs, HPAPI, NCEs and novel advanced intermediates
Complimentary techniques for determining relative response factor of non- isolated impurities
Understanding the concept behind determining UV RRF of non-isolated impurities using High Performance Liquid Chromatography and Nuclear Magnetic Resonance
The many benefits of outsourcing Stability: A Baxter-Syngene Case study
Learn why Baxter chose to partner with Syngene for Stability studies, the business flow, governance mechanism and metrics that were implemented, which enabled a mutually successful collaboration.
Audit Syngene Virtually
Syngene is using virtual audits to enable clients/regulators experience its capability and infrastructure, without physically visiting the site.
Multidrug combo for companion animals
Learn how Syngene developed and commercialized for its client, a complex palatable dosage form comprising three actives for use in companion animals.
Combating COVID-19 – The Oligonucleotide Way
Synthetic oligonucleotides have emerged as an important modality for diagnostics and potential therapy option for COVID-19.