Literature DB >> 24218058

Quality-by-design: are we there yet?

Jack Cook1, Maria T Cruañes, Manish Gupta, Steve Riley, John Crison.   

Abstract

In 2012, the Quality-by-Design and Product Performance Focus Group of AAPS conducted a survey to assess the state of adoption and perception of Quality-by-Design (QbD). Responses from 149 anonymous individuals from industry-including consultants-(88%), academia (7%), and regulatory body (4%), were collected. A majority of respondents (54% to 76%) reported high frequency of utilization of several tools and most QbD elements outlined by International Conference on Harmonization Q8, with design of experiments, risk assessment, and the quality target product profile ranked as the top three. Over two thirds of respondents agreed that the benefits of QbD included both the positive impact it can have on the patient (78%), as well as on internal processes such as knowledge management (85%), decision making (79%), and lean manufacture (71%). However, more than 50% from industry were neutral about or disagreed with QbD leading to a better return on investment. This suggests that, despite the recognized scientific, manufacture, and patient-related benefits, there is not yet a clearly articulated business case for QbD available. There was a difference of opinion between industry and regulatory agency respondents as to whether a QbD-based submission resulted in increased efficiency of review. These contrasting views reinforce the idea that QbD implementation can benefit from further dialog between industry and regulatory authorities. A majority of respondents from academia indicated that QbD has influenced their research. In total, the results indicate the broad adoption of QbD but also suggest we are yet in a journey and that the process of gathering all experience and metrics required for connecting and demonstrating QbD benefits to all stakeholders is still in progress.

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Year:  2013        PMID: 24218058      PMCID: PMC3909153          DOI: 10.1208/s12249-013-0043-1

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  5 in total

1.  Summary workshop report: Facilitating oral product development and reducing regulatory burden through novel approaches to assess bioavailability/bioequivalence.

Authors:  James E Polli; Jack A Cook; Barbara M Davit; Paul A Dickinson; Domenick Argenti; Nancy Barbour; Alfredo García-Arieta; Jean-Marie Geoffroy; Kerry Hartauer; Shoufeng Li; Amitava Mitra; Francis X Muller; Vivek Purohit; Manuel Sanchez-Felix; John W Skoug; Kin Tang
Journal:  AAPS J       Date:  2012-06-09       Impact factor: 4.009

2.  Meeting report: applied biopharmaceutics and quality by design for dissolution/release specification setting: product quality for patient benefit.

Authors:  Arzu Selen; Maria T Cruañes; Anette Müllertz; Paul A Dickinson; Jack A Cook; James E Polli; Filippos Kesisoglou; John Crison; Kevin C Johnson; Gordon T Muirhead; Timothy Schofield; Yi Tsong
Journal:  AAPS J       Date:  2010-06-02       Impact factor: 4.009

Review 3.  Statistical thinking and knowledge management for quality-driven design and manufacturing in pharmaceuticals.

Authors:  Evdokia Korakianiti; Dimitrios Rekkas
Journal:  Pharm Res       Date:  2010-12-14       Impact factor: 4.200

Review 4.  Clinical relevance of dissolution testing in quality by design.

Authors:  Paul A Dickinson; Wang Wang Lee; Paul W Stott; Andy I Townsend; John P Smart; Parviz Ghahramani; Tracey Hammett; Linda Billett; Sheena Behn; Ryan C Gibb; Bertil Abrahamsson
Journal:  AAPS J       Date:  2008-08-07       Impact factor: 4.009

5.  Draft guidance for industry extended-release solid oral dosage forms. Development, evaluation and application of in vitro-in vivo correlations.

Authors:  H Malinowski; P Marroum; V R Uppoor; W Gillespie; H Y Ahn; P Lockwood; J Henderson; R Baweja; M Hossain; N Fleischer; L Tillman; A Hussain; V Shah; A Dorantes; R Zhu; H Sun; K Kumi; S Machado; V Tammara; T E Ong-Chen; H Mahayni; L Lesko; R Williams
Journal:  Adv Exp Med Biol       Date:  1997       Impact factor: 2.622

  5 in total
  2 in total

Review 1.  Role of Knowledge Management in Development and Lifecycle Management of Biopharmaceuticals.

Authors:  Anurag S Rathore; Oscar Fabián Garcia-Aponte; Aydin Golabgir; Bibiana Margarita Vallejo-Diaz; Christoph Herwig
Journal:  Pharm Res       Date:  2016-10-26       Impact factor: 4.200

2.  Implementation of Quality by Design (QbD) Principles in Regulatory Dossiers of Medicinal Products in the European Union (EU) Between 2014 and 2019.

Authors:  Judith P Ter Horst; Sada L Turimella; Frans Metsers; Alex Zwiers
Journal:  Ther Innov Regul Sci       Date:  2021-01-13       Impact factor: 1.778

  2 in total

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