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News / Sep 10, 2021

67 Voices for Portugal - The Great Opportunity

Book Presentation Debate

book 67 vozes guy villax hovione

? What’s crucial to recover the Portuguese economy? 

 

Guy Villax, Hovione's CEO, joins a group of 67 Portuguese Leaders to write the book 67 VOICES FOR PORTUGAL – THE GREAT OPPORTUNITY, an initiative of Iscte Executive Education with 67 texts about the future of Portugal in the pandemic context. Guy Villax is once again acknowledged as a reference in the business world in connection to innovation and knowledge, by being asked to share his vision for the future of Portugal.

 

Guy Villax - EY World Entrepreneur Of The Year™ 2021 | Hovione

​​​​​​​In the chapter “Map for a rebirth” signed by Guy Villax, he addresses the need for “simple, clear, steady policies with a long-term view. We need a consensus as regards the model for economic growth (that means a non-partisan model), that leverages on our competitive advantages and strengths”.

 

Read here Guy Villax's full text.

 

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Continuous Tableting (CT) is defined as continuous manufacturing of oral dose drugs, specifically tablets. As per ICH's Q13 definition1, a continuous manufacturing process in the pharmaceutical industry comprises at least two unit operations integrated from a mechanical and software perspective. There is a wide combination of possible CT process configurations that are dependent on the needs of the intended product formulation and each of the individual unit operations that constitute the process train can be continuous, semi-continuous, or batch processes. The typical manufacturing processes for tablet formulation are direct compression (DC), dry granulation (DG) and wet granulation (WG)2 - details on these manufacturing processes are beyond the scope of this article, so the interested reader is directed to relevant literature. The actual implementation of CT technology in a facility can broadly vary depending on the level of desired integration and automation. Process trains can be designed to be flexible and converted between multiple configurations (e.g. continuous DC, DG and WG), controlled by the end user from one single software and within a single clean room. The other possibility would be for subsections of the CT process to be divided into multiple clean rooms where inprocess materials are transferred between suites via a bin-to-bin approach (e.g. a granulation suite to prepare granules from raw materials followed by continuous DC (CDC) to blend the granules and produce tablets). The level of automation and instrumentation designed into the CT process (typically involving Process Analytical Technologies, PAT) can open the possibility to implement sophisticated control strategies. Key components of a control strategy that need to be considered for CT are material tracking and genealogy, knowledge of the residence time distribution (RTD), and in-process controls (spectroscopic and/or soft sensors based on process parameters). Holistically, these control strategy elements enable the implementation of a material diversion strategy to automatically divert out of specification material from the process. In their most advanced form, control strategies may also enable real time release testing (RTRt) of the final tablet drug product and reduce the off-line analytical burden and the number of operators needed to manage the process.   Read the full article at gmp-journal.com  

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