An adequate quality product development in a timely manner is a critical issue of the pharma business. Planning and developing finished products is performed in a thorough way. Continuous linkage with our clients and partners ensures a final dosage form meeting patient compliance and our clients’ corporate objectives.
At LEF each drug and excipient goes through a customized pre-formulation characterization to identify the best formulation strategy for each product.
- Excipient screening;
- Compatibility evaluation between the several formulation components.
Formulation development and Manufacturing
Each product is unique. The integration of pre-formulation data with a careful formulation development plan allows the efficient development of robust easily manufacturable drug products.
Flexibility is crucial. Our pilot scale production unit is prepared to produce small batches of non-sterile solid, semi-solids and liquid dosage forms, under full GMP environment.
- Prototype Development;
- Formulation Optimization;
- Pilot scale manufacturing;
- Scale up support;
- Supporting Documentation;
- Industrial transfer and production site procurement is also available.