STEERLife provides integrated Contract Research Organization (CRO) services supporting pharmaceutical development from early feasibility assessment through regulatory readiness.
Our scientific expertise and advanced formulation technologies enable efficient development of complex and difficult-to-formulate drug products while maintaining strong analytical and regulatory support.
Comprehensive research and formulation development support focused on complex pharmaceutical products and scalable outcomes.
Scalable manufacturing support enabling seamless technology transfer and execution of pilot and pivotal batch programs.
Regulatory coordination and documentation support designed to streamline submissions and development timelines.
Feasibility trials assess whether a formulation or process can be successfully developed and scaled, minimizing risks before full-scale development.
Patent landscaping involves analyzing existing patents and technology trends. It helps organizations to identify opportunities, avoid infringement, and guide product development strategies.
ASD development is a pharmaceutical approach used to improve the solubility and bioavailability of poorly soluble drugs through optimized formulation techniques.
Yes, we provide support with API sourcing and also help with RLD procurement, ensuring compliance with regulatory requirements.
Technology transfer ensures a smooth transition of processes from development to manufacturing scale while maintaining product quality and consistency.
Yes, we offer contract manufacturing and supply of finished dosage forms (FDFs) to support your commercial requirements, but not as a stand-alone service. For partners who are licensing from us, we offer product supply from a partner CMO site, either in the form of supply of intermediate granules or as FDFs (finished dosage forms).
Yes, we coordinate BE studies and help select appropriate partners to ensure successful study execution.
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