Analytical method development and optimization refers to a process established series analysis methods and procedures during the drug research and development process to better understand the properties of the drug, including the physical properties, chemical properties, biological properties, etc., of the drug, which ensure that the drug meets relevant quality standards and regulatory requirements. https://www.formulationbio.com/novel-delivery/pharmaceutical-analytical-method-development-and-optimization.html

Active pharmaceutical ingredients (APIs) are the basis for drugs to exert pharmacological activity, and can be produced by chemical synthesis, plant extraction or biotechnology. Relying on our professional technical team and cutting-edge technology platform, CD Formulation provides a variety of APIs, and offers customized services according to customer needs. https://www.formulationbio.com/products/active-pharmaceutical-ingredient-excipients.html

Stability analysis of microspheres is of great significance and value for their use as drug carriers. The stability analysis can be used to better understand the preservation pathway, preservation environment and shelf life of microspheres. It can also be used to analyze the effect of solvent, pH, and temperature on the microspheres when loaded with drugs. After the stability analysis, https://msmn.formulationbio.com/microsphere-stability-testing.html

Oral thin films are a very thin polymer films, consisting of a single or multi-layer polymer matrix, which are usually applied in the mouth to function. Oral thin films are usually water-based soluble polymers designed for rapid and systematic delivery of drugs, with the active substance transported directly into the bloodstream. This avoids exposing the drug to the harsh conditions of the stomach and allows this drug delivery system to deliver a greater percentage of the active compound per dose. https://www.formulationbio.com/oral-thin-films-technology-services.html