Bringing a pharmaceutical product to life requires more than just active ingredients—it demands vision, precision, and the right partner by your side. At Suanfarma, we collaborate with pharmaceutical and biotech companies to co-develop differentiated products, offer regulatory and strategic consulting, and provide or connect you with tailored CDMO solutions that match your project’s needs.
Collaborating Beyond APIs
Flexibility is at the core of how we develop solutions. Our co-development services are built to adapt—whether you’re starting from an early-stage concept or looking to optimize a product close to launch.
With in-house capabilities and a strong network of trusted CDMOs, we help manage the full development cycle:
- Feasibility and formulation support
- Technology transfer and industrial scale-up
- Regulatory strategy and dossier preparation
- Manufacturing solutions aligned with your timeline and goals
With decades of regulatory and commercial insight, we support our partners in making the right decisions at every stage of development—whether it’s navigating complex market access, defining a strong product strategy, or preparing documentation for highly regulated markets.
This includes guidance on:
- Regulatory planning and compliance
- Product and portfolio evaluation
- Scientific and technical assessments
- Supply chain optimization and readiness
At Suanfarma, we bring together integrated capabilities that span from early development to final delivery. Whether through our own CDMO services or by identifying the right partner for each project, we ensure tailored solutions that fit your needs. Our experience across 70+ regulatory markets allows us to navigate complexity with confidence, while our way of working—transparent, agile, and collaborative—helps turn ideas into impactful outcomes. Let’s build the next solution together.
