Pre-formulation
At LEF each drug and excipient goes through a customized pre-formulation characterization to identify the best formulation strategy for each product.
- Pre-formulation
- Solubility/permeability and stability evaluation
- Comprehensive excipient screening
Formulation development and Production
Each product is unique. At our pilot plant unit, the integration of pre-formulation data with a careful formulation development plan will allow the efficient development of robust, easily manufacturable drug products.
Flexibility is crucial. We are prepared to produce small batches of non sterile solid, semi-solids and liquid dosage forms, including clinical supplies for clinical trials, under full cGMP conditions.
- Prototype Development
- Formulation Optimization
- Pilot scale manufacturing of non sterile solid, semi-solids and liquid dosage forms
- Biobatch manufacturing and clinical supplies
- Scale up support
- Full data documentation
Throughout the development process a close collaboration is maintained with our clients. Emphasis is put on providing all the relevant information at each developing step. Our goal is to achieve a final dosage form that ensures patient compliance and our customers corporate objectives.