Literature DB >> 32467177

Industry One-Voice-of-Quality (1VQ) Solutions: Effective Management of Post-Approval Changes in the Pharmaceutical Quality System (PQS)-through Enhanced Science and Risk-Based Approaches.

Emma Ramnarine1, Anders Vinther2, Kimberly Bruhin3, Christina Tovar4, Marcello Colao5.   

Abstract

Post-approval changes are inevitable and necessary throughout the life of a drug product-to implement new knowledge, maintain a state of control, and drive continual improvement. Many post-approval changes require regulatory agency approval by individual countries before implementation. Because of the global regulatory complexity, individual post-approval changes usually take years for full worldwide approval even when they reduce patient risk, improve compliance, or enhance the manufacturing process or test methods. This global complexity slows down continual improvement and innovation and can cause drug shortages and current good manufacturing practices compliance issues. Manufacturers that market products globally experience the greatest challenge and risks in their daily operations because of this post-approval change complexity. A global problem needs a global solution. This paper has been sponsored and endorsed by senior quality leaders (Chief Quality Officers/Heads of Quality) from >20 global pharmaceutical companies who have collaborated to speak with "One-Voice-Of-Quality" (1VQ). The paper provides two specific solutions that lay the foundation for an aligned and standardized industry position on the topic of effective management of post-approval changes in the pharmaceutical quality system (PQS). This document represents the 1VQ standard approach for the steps necessary to establish and demonstrate an effective quality system to fully leverage a risk-based approach to post-approval changes as laid out by ICH Q10 Annex 1. Implementation of the solutions presented in this paper can help achieve a transformational shift with faster implementation of new knowledge, continual improvement, and innovation through post-approval changes. The Chief Quality Officers/Heads of Quality are inviting other companies to join the 1VQ (contact either Emma Ramnarine or Anders Vinther) and other stakeholders to join the dialog. © PDA, Inc. 2020.

Entities:  

Keywords:  ICH Q10; ICH Q12; Pharmaceutical quality system (PQS); Pharmaceuticals; Post-approval change (PAC); Science and risk-based approach

Mesh:

Substances:

Year:  2020        PMID: 32467177     DOI: 10.5731/pdajpst.2020.011734

Source DB:  PubMed          Journal:  PDA J Pharm Sci Technol        ISSN: 1079-7440


  3 in total

Review 1.  How to accelerate the supply of vaccines to all populations worldwide? Part II: Initial industry lessons learned and detailed technical reflections leveraging the COVID-19 situation.

Authors:  Mic McGoldrick; Thierry Gastineau; Diane Wilkinson; Cristiana Campa; Norbert De Clercq; Andrea Mallia-Milanes; Olivier Germay; Jyothsna Krishnan; M Van Ooij; Michael P Thien; Peter J Mlynarczyk; Edward Saltus; Florence Wauters; Philippe Juvin; Didier Clenet; Ana Basso; Nora Dellepiane; Sonia Pagliusi; Monique Collaço de Moraes Stávale; Venkatraman H Sivaramakrishnan; Samir Desai
Journal:  Vaccine       Date:  2022-02-23       Impact factor: 3.641

Review 2.  How to accelerate the supply of vaccines to all populations worldwide? Part I: Initial industry lessons learned and practical overarching proposals leveraging the COVID-19 situation.

Authors:  Mic McGoldrick; Thierry Gastineau; Diane Wilkinson; Cristiana Campa; Norbert De Clercq; Andrea Mallia-Milanes; Olivier Germay; Jyothsna Krishnan; M Van Ooij; Michael P Thien; Peter J Mlynarczyk; Edward Saltus; Philippe Juvin; Didier Clenet; Ana Basso; Nora Dellepiane; Sonia Pagliusi; Monique Collaço de Moraes Stávale; Venkatraman H Sivaramakrishnan; Samir Desai
Journal:  Vaccine       Date:  2022-02-23       Impact factor: 3.641

3.  Path Forward to Optimise Post-approval Change Management and Facilitate Continuous Supply of Medicines and Vaccines of High Quality Worldwide : Joint Position from EFPIA, IFPMA and Vaccines Europe.

Authors:  Andrew Deavin; Sarah Adam; Susanne Ausborn; Ane Sofie Böhm Nielsen; Sonia Cappellini; Isabelle Colmagne-Poulard; Thierry Gastineau; Arturo Gonzalez-Martinez; Sylvie Meillerais; Charlie Mortazavi
Journal:  Ther Innov Regul Sci       Date:  2022-08-02       Impact factor: 1.337

  3 in total

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