Oral dosage form development is a process that uses active pharmaceutical ingredients (APIs) and excipients to make a dosage form of a drug suitable for oral administration. The performance of the dosage form can be controlled or optimized by changing the physical and chemical properties of the excipient and coating. Excipients can help define the bioavailability, release characteristics, and stability of the formulation, and coatings can influence where and how quickly the drug is released in the body. Oral dosage forms can be in the form of tablets, capsules, granules, liquids, etc., each with different development and preparation requirements. Learn more about oral dosage form development: https://www.alfa-apisector.com/oral-dosage-form-development.html