Literature DB >> 22749874

Strategic funding priorities in the pharmaceutical sciences allied to Quality by Design (QbD) and Process Analytical Technology (PAT).

Buket Aksu1, Thomas De Beer, Staffan Folestad, Jarkko Ketolainen, Hans Lindén, Joao Almeida Lopes, Marcel de Matas, Wim Oostra, Jukka Rantanen, Marco Weimer.   

Abstract

Substantial changes in Pharmaceutical R&D strategy are required to address existing issues of low productivity, imminent patent expirations and pressures on pricing. Moves towards personalized healthcare and increasing diversity in the nature of portfolios including the rise of biopharmaceuticals however have the potential to provide considerable challenges to the establishment of cost effective and robust supply chains. To guarantee product quality and surety of supply for essential medicines it is necessary that manufacturing science keeps pace with advances in pharmaceutical R&D. In this position paper, the EUFEPS QbD and PAT Sciences network make recommendations that European industry, academia and health agencies focus attention on delivering step changes in science and technology in a number of key themes. These subject areas, all underpinned by the sciences allied to QbD and PAT, include product design and development for personalized healthcare, continuous-processing in pharmaceutical product manufacture, quantitative quality risk assessment for pharmaceutical development including life cycle management and the downstream processing of biopharmaceutical products. Plans are being established to gain commitment for inclusion of these themes into future funding priorities for the Innovative Medicines Initiative (IMI).
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22749874     DOI: 10.1016/j.ejps.2012.06.009

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  5 in total

1.  Development of a quantitative mass spectrometry multi-attribute method for characterization, quality control testing and disposition of biologics.

Authors:  Richard S Rogers; Nancy S Nightlinger; Brittney Livingston; Phil Campbell; Robert Bailey; Alain Balland
Journal:  MAbs       Date:  2015-07-17       Impact factor: 5.857

Review 2.  Hot-Melt Extrusion: from Theory to Application in Pharmaceutical Formulation.

Authors:  Hemlata Patil; Roshan V Tiwari; Michael A Repka
Journal:  AAPS PharmSciTech       Date:  2015-07-10       Impact factor: 3.246

3.  Automated multi-attribute method sample preparation using high-throughput buffer exchange tips.

Authors:  Yuko Ogata; Pamela M Quizon; Nancy S Nightlinger; Pongkwan Sitasuwan; Casey Snodgrass; L Andrew Lee; Jeffrey D Meyer; Richard S Rogers
Journal:  Rapid Commun Mass Spectrom       Date:  2022-01-30       Impact factor: 2.586

Review 4.  The Future of Pharmaceutical Manufacturing Sciences.

Authors:  Jukka Rantanen; Johannes Khinast
Journal:  J Pharm Sci       Date:  2015-08-17       Impact factor: 3.534

Review 5.  Sol-gel Silica Nanoparticles in Medicine: A Natural Choice. Design, Synthesis and Products.

Authors:  M Clara Gonçalves
Journal:  Molecules       Date:  2018-08-13       Impact factor: 4.411

  5 in total

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