A systematic framework and software are needed to implement material traceability in continuous pharmaceutical tablet manufacturing. Pharmaceutical manufacturing is an area with strict regulations ...

Steve Osborn, product design manager at tablet tooling manufacturer I Holland, spoke to Pharmaceutical Technology Europe about the key considerations for successful implementation of multi-tip tooling ...

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 ...

Tablets were first developed in the mid-1850s, during which sugar coating (SC) was primarily used to improve their surface characteristics and protect pharmaceutical agents from the harsh environment ...

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 ...

Background Enhancing the flexibility of operations is now a major priority for pharmaceutical manufacturers so they can quickly adapt to change & accommodate a wider range of products (inc.

This interactive workshop provides up-to-date, relevant and detailed information on the impact of Quality by Design (QbD) on the Development and Validation of tablet manufacturing processes. It will ...