Seamlessly from concept to clinical supply
We offer end-to-end formulation development services for solid oral dosage forms, supporting pharmaceutical companies from early-stage concept through to clinical trial supply. Our approach combines deep scientific expertise with advanced technologies to create customized, scalable, and regulatory-compliant formulations.
Our formulation development services include:
- Pre-formulation and excipient screening to identify optimal ingredient combinations for stability, performance, and manufacturability.
- Prototype development using enabling technologies such as hot melt extrusion, spray drying, and EUDRATEC® platforms.
- Controlled release, enteric protection, and targeted delivery solutions tailored to your drug’s pharmacokinetic profile and therapeutic goals.
- Process development and scale-up under GMP conditions to ensure smooth transition from lab to clinical manufacturing.
- Analytical method development and stability testing to support regulatory submissions and quality assurance.
Our scientists work closely with your team to design oral formulations that address key challenges such as poor solubility, low bioavailability, gastrointestinal degradation, and patient compliance. Whether you’re developing a new molecule or improving an existing product, we provide the technical insight and infrastructure to accelerate your path to market.