Syngene’s Small Molecule cGMP commercial manufacturing facility
Syngene’s state-of-the-art small molecule cGMP manufacturing facility is USFDA and PMDA-approved. The facility manufactures clinical (early and late-phase) and commercial drug substances (NCEs), advanced intermediates, regulatory starting materials, and selected generic APIs for clients. The facility’s manufacturing output ranges from grams to hundreds of kilograms per batch, with total volumes ranging from 60L to 8000L.
Syngene’s high potent API manufacturing facility
Our high potent API facility is designed to handle cytotoxic and cytostatic high-potency compounds with a commitment to safety.
How Syngene supported a large pharma company in generating gene knockouts in iPSCs with >95% efficiency
Learn how Syngene helped generate human iPSCs gene knockouts with >95% efficiency for an allogeneic cell and gene therapy.
Cracking the Code: Transformative role of pDNA in advanced modalities
Reasons behind the rise in demand for pDNA and what to look for in a pDNA engineering and manufacturing partner when deciding to outsource.
Pharma Supply Chain: From Fragile to Agile
CDMOs bolster supply networks with additional capabilities to make themselves resilient to potential challenges and ensure secure supplies to customers.
Quality management paradigm shift: Risk-centric practices come center stage
CDMOs have moved to risk-based quality management systems comprising highly integrated and digitalized processes powered by data to ensure drug quality.
Protein therapeutics to amp up outsourcing in animal health
With the boom in pet ownership and rising awareness about pet health, veterinary drug makers are betting big on protein therapeutics and outsourcing biologics development to CDMOs.
Establishing the simple complex: Route to a successful large molecule bioanalytical sample analysis
Learn the simple and complex connections that must be established for successful large molecule bioanalytical sample analysis supporting clinical trials.
Syngene Quality Control Biologics Lab
Our Quality Control Biologics lab uses the latest technology and equipment for testing biologics products, with a strong focus on digitalization and automation. Our stringent quality control procedures and standards ensure the accuracy and reliability of results. Further, we are one of the pioneers of real-wear-assisted reality glasses for collaborative technology transfer and hosting remote inspections in alignment with FDA guidelines.
How Syngene’s Green Chemistry initiatives reduced costs by 30% while increasing yield and reducing wastage
Learn how Syngene developed a robust and scalable Green GMP manufacturing process for an oncology drug compound in just eight weeks, which reduced costs by 30%.