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 ...

This unique 2 day course introduces and integrates the key elements of tablet development based on the principles of Quality by Design (QbD) set out in ICH Q9. It will include experimental, hands-on ...

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 ...

Normally this wouldn't be cause for concern but when a tablet is marketed as being splash proof, it should live up to those claims. A fault in the manufacturing process has created a small gap between ...

Historically, pharmaceutical products have been produced in a traditional ‘batch’ system, in which every operation is executed separately using a defined quantity of materials. In batch manufacturing ...