A Review of PAT Strategies in Secondary Solid Oral Dosage Manufacturing of Small Molecules

Author:

Laske Stephan,Paudel Amrit,Scheibelhofer Otto,Sacher Stephan,Hoermann Theresa,Khinast Johannes,Kelly Adrian,Rantannen Jukka,Korhonen Ossi,Stauffer Fanny,De Leersnyder Fien,De Beer Thomas,Mantanus Jerome,Chavez Pierre-Francois,Thoorens Benjamin,Ghiotti Patrizia,Schubert Martin,Tajarobi Pirjo,Haeffler Gunnar,Lakio Satu,Fransson Magnus,Sparen Anders,Abrahmsen-Alami Susanna,Folestad Staffan,Funke Adrian,Backx Ivo,Kavsek Barbara,Kjell Francois,Michaelis Marc,Page Trevor,Palmer John,Schaepman Alexander,Sekulic Sonja,Hammond Steve,Braun Birgit,Colegrove Brenda

Funder

Austrian Federal Ministry of Transport, Innovation and Technology

Austrian Federal Ministry of Economy, Family and Youth

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference248 articles.

1. Process Analytical Technology for continuous manufacturing of solid-dosage forms;Fonteyne;TRAC Trends Anal Chem,2015

2. Guidance for Industry. PAT—A Framework for Innovative Pharmaceutical Development, Manufacturing and Quality Assurance,2004

3. International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. Pharm Development Q8(R2). Vol. 2. International Conference on Harmonization,2009

4. Assessment of recent process analytical technology (PAT) trends: a multiauthor review;Simon;Org Process Res Dev,2015

5. Making Medicines: A Brief History of Pharmacy and Pharmaceuticals,2005

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