At STEERLife, pharmaceutical development begins with the end in mind – commercial manufacturing.
We partner with customers across the entire journey integrating formulation science, process engineering and commercialization into one seamless development pathway.
Every project is designed to minimize development risk, simplify technology transfer and accelerate commercial success with robust, scalable manufacturing processes.
Better formulations begin with better understanding of the molecule. We engineer formulations for Solubility and bioavailability enhancement, Controlled and modified drug release, Amorphous solid dispersions, Highly potent and low-dose formulations, Continuous granulation, melt processing, Improved manufacturability and commercial scalability.
At STEER, formulation scientists and process engineers work together from Day 1 establish process understanding, robust operating windows and commercially relevant manufacturing strategies.
Our integrated approach includes:
One Partner. One Seamless path to Commercial Success.
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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Changing the Way we Make and Take Medicines.
