Adopting a Quality by Design (QbD) approach for wet granulation requires manufacturers to comprehend the correlation between process variables, such as powder characteristics and equipment ...

The goal of this workshop is to provide detailed information on the implications of Quality by Design (QbD) for the validation and qualification of tablet manufacturing processes and process ...

A pharmaceutical tablet is defined as a solid dosage form containing drug material normally with suitable diluents and prepared either by compression or molding methods. Drug formulation and design ...

Moisture content determination is an important quality control test in pharmaceutical manufacturing, from the checking of incoming raw materials and in-process control of tablets and capsules to ...

Continuous processing as described by the regulatory agencies is the pharmaceutical industry’s area of focus in order to enhance product quality and productivity. It is essential to understand the ...

What is Real-Time Release Testing? Real-Time Release Testing (RTRT) is an advanced approach to biopharmaceutical manufacturing quality control that improves upon current systems. RTRT is defined as ...