Defects tablet during manufacturing

In the manufacturing process, tablet defects can arise from problems with the core components of the tablet, such as lump formation or poor compressibility. Tablet defects can also be caused by defects in the extrusion process, such as air bubbles or tears in the film. Finally, tablet defects may occur during the finishing process, such as tablet cracking or creasing.

Tablet defects can have a significant impact on the quality of a pharmaceutical product. They can cause tablets to fail at various stages of their manufacturing process, resulting in lower yields and higher costs. In some cases, defective tablets can even cause patient safety issues.

To avoid problems with tablet defects in pharmaceutical manufacturing, it is important to carefully measure and account for all potential error sources during the manufacturing process. This will help ensure that your products meet customer expectations and are defect-free.

To prevent these errors from occurring in the first place, manufacturers must take several steps. This includes using high-quality materials and equipment, as well as strict quality control procedures. By doing this, they can ensure that their tablets meet all customer expectations and are safe to use

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