Literature DB >> 28579542

Modeling in the quality by design environment: Regulatory requirements and recommendations for design space and control strategy appointment.

Jelena Djuris1, Zorica Djuric2.   

Abstract

Mathematical models can be used as an integral part of the quality by design (QbD) concept throughout the product lifecycle for variety of purposes, including appointment of the design space and control strategy, continual improvement and risk assessment. Examples of different mathematical modeling techniques (mechanistic, empirical and hybrid) in the pharmaceutical development and process monitoring or control are provided in the presented review. In the QbD context, mathematical models are predominantly used to support design space and/or control strategies. Considering their impact to the final product quality, models can be divided into the following categories: high, medium and low impact models. Although there are regulatory guidelines on the topic of modeling applications, review of QbD-based submission containing modeling elements revealed concerns regarding the scale-dependency of design spaces and verification of models predictions at commercial scale of manufacturing, especially regarding real-time release (RTR) models. Authors provide critical overview on the good modeling practices and introduce concepts of multiple-unit, adaptive and dynamic design space, multivariate specifications and methods for process uncertainty analysis. RTR specification with mathematical model and different approaches to multivariate statistical process control supporting process analytical technologies are also presented.
Copyright © 2017 Elsevier B.V. All rights reserved.

Keywords:  Control strategy; Design space; Mathematical modeling; Pharmaceutical manufacturing; Quality by design; Real-time release

Mesh:

Year:  2017        PMID: 28579542     DOI: 10.1016/j.ijpharm.2017.05.070

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  6 in total

1.  Digital Twins and Their Role in Model-Assisted Design of Experiments.

Authors:  Kim B Kuchemüller; Ralf Pörtner; Johannes Möller
Journal:  Adv Biochem Eng Biotechnol       Date:  2021       Impact factor: 2.635

2.  Scale-Up Strategy in Quality by Design Approach for Pharmaceutical Blending Process with Discrete Element Method Simulation.

Authors:  Su Bin Yeom; Du Hyung Choi
Journal:  Pharmaceutics       Date:  2019-06-06       Impact factor: 6.321

3.  Control Strategy for Process Development of High-Shear Wet Granulation and Roller Compaction to Prepare a Combination Drug Using Integrated Quality by Design.

Authors:  Ji Yeon Kim; Myung Hee Chun; Du Hyung Choi
Journal:  Pharmaceutics       Date:  2021-01-08       Impact factor: 6.321

Review 4.  Design Space and QbD Approach for Production of Drug Nanocrystals by Wet Media Milling Techniques.

Authors:  Leena Peltonen
Journal:  Pharmaceutics       Date:  2018-07-25       Impact factor: 6.321

5.  A Novel Framework to Aid the Development of Design Space across Multi-Unit Operation Pharmaceutical Processes-A Case Study of Panax Notoginseng Saponins Immediate Release Tablet.

Authors:  Fei Sun; Bing Xu; Shengyun Dai; Yi Zhang; Zhaozhou Lin; Yanjiang Qiao
Journal:  Pharmaceutics       Date:  2019-09-13       Impact factor: 6.321

Review 6.  Direct Compaction Drug Product Process Modeling.

Authors:  Alexander Russell; John Strong; Sean Garner; William Ketterhagen; Michelle Long; Maxx Capece
Journal:  AAPS PharmSciTech       Date:  2022-01-31       Impact factor: 3.246

  6 in total

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