Review Article - Global Research Online

1 Int. J. pharm . Sci. Rev. Res., 17(2), 2012; n 04, 20-28 ISSN 0976 044X. Review Article QUALITY BY DESIGN (QBD) : A COMPLETE Review . Nishendu P. Nadpara*, Rakshit V. Thumar, Vidhi N. Kalola, Parula B. Patel Department of Quality Assurance, S. J. Thakkar Pharmacy College, Opp. Drivein cinema, Avadh Road, Rajkot, Gujarat, India. *Corresponding author's E-mail: Accepted on: 02-10-2012; Finalized on: 30-11-2012. ABSTRACT. Quality by Design is the modern approach for quality of pharmaceuticals. This paper gives idea about the Pharmaceutical Quality by Design (QbD) and describes use of Quality by Design to ensure quality of Pharmaceuticals. The Quality by Design is described and some of its elements identified. Process parameters and quality attributes are identified for each unit operation. Benefits, opportunities and steps involved in Quality by Design of Pharmaceutical products are described.

2 The aim of the pharmaceutical development is to design a quality product and its manufacturing process to consistently deliver the intended performance of the product. Quality cannot be tested into products but quality should be built in by design. It includes the Quality target product profile, critical quality attributes and key aspects of Quality by Design. It also gives comparison between product quality by end product testing and product quality by Quality by Design. The foundation of Quality by Design is ICH Guidelines. It is based on the ICH Guidelines Q8 for pharmaceutical development, Q9 for quality risk management, Q10 for pharmaceutical quality systems. It also gives application of Quality by Design in pharmaceutical development and manufacturing of pharmaceuticals. Keywords: Quality by Design (QbD), Process Analytical Technology (PAT), Quality target product profile, Critical quality attributes.

3 INTRODUCTION include, for example, incorporation of prior knowledge, results of studies using design of experiments, use of The aim of pharmaceutical development is to design a quality risk management, and use of knowledge quality product and its manufacturing process to management (ICH Q10) throughout the lifecycle of the consistently deliver the intended performance of the product. Such a systematic approach can enhance product. The information and knowledge gained from achieving the desired quality of the product and help the pharmaceutical development studies and manufacturing regulators to better understand a company's strategy. experience provide scientific understanding to support Product and process understanding can be updated with the establishment of the design space, specifications, and the knowledge gained over the product lifecycle.

4 1-5. manufacturing controls. Information from pharmaceutical development studies can be a basis for quality risk Design4, 5. management. It is important to recognize that quality Product is designed to meet patient needs and cannot be tested into products; , quality should be performance requirements. built in by design. Changes in formulation and manufacturing processes during development and Process is designed to consistently meet product lifecycle management should be looked upon as quality attributes. opportunities to gain additional knowledge and further support establishment of the design space. Similarly, Impact of starting raw materials and process inclusion of relevant knowledge gained from experiments parameters on product quality is understood. giving unexpected results can also be useful. Design space Critical sources of process variability are identified and is proposed by the applicant and is subject to regulatory controlled.

5 Assessment and approval. Working within the design space is not considered as a change. Movement out of the The process is continually monitored and updated to design space is considered to be a change and would allow for consistent quality over time. normally initiate a regulatory post approval change Definition [ICH Q 8(R1)]. process. A systematic approach to development that begins with In all cases, the product should be designed to meet predefined objectives and emphasizes product and patients' needs and the intended product performance. process understanding and process control, based on Strategies for product development vary from company to 6. sound science and quality risk management. company and from product to product. The approach can also vary and should be outlined in the submission. An Definition [FDA PAT Guidelines, Sept.]

6 2004]. applicant might choose either an empirical approach or a A system for designing, analyzing and controlling more systematic approach to product development, or a manufacturing through timely measurements ( during combination of both. A more systematic approach to processing) of critical quality and performance attributes development (also defined as quality by design) can International Journal of Pharmaceutical Sciences Review and Research Page 20. Available Online at Int. J. pharm . Sci. Rev. Res., 17(2), 2012; n 04, 20-28 ISSN 0976 044X. of new and in-process materials and processes, with the 3. Control Strategy goal of ensuring final product safety. 5, 6. Risk based decision The concept of Quality by Design (QbD) was defined as Continuous Improvement an approach which covers a better scientific understanding of critical process and product qualities, Product performance designing controls and tests based on the scientific limits of understanding during the development phase and Seven steps of quality by design start up plan using the knowledge obtained during the life-cycle of the 1.

7 Hire an independent Quality by design expert. product to work on a constant improvement 2. Audit your organization and process with the expert environment. QbD describes a pharmaceutical development approach referring to formulation design conducting a gape analysis. and development and manufacturing processes to 3. Hold a basic quality by design workshop with all your maintain the prescribed product quality. Guidelines and personal. mathematical models are used to ensure the 4. Review the expert's report and recommendation. establishment and use of the knowledge on the subject in an independent and integrated way. 5. Draft an implementation plan, timelines and estimated 1,3,5,6 costs. Benefits of QBD. 6. Assign the resources (or contract out). QbD is good Business 7. Retain the independent expert as your Project Eliminate batch failures Assurance advisor.

8 Minimize deviations and costly investigations Quality by design (QbD) and well understood product Avoid regulatory compliance problems and processes4,7,8. Organizational learning is an investment in the future All critical sources of variability are identified and explained. QbD is good Science Variability is controlled by the process. Better development decisions Product quality attributes can be accurately and Empowerment of technical staff reliably predicted over the design space established Opportunities7,8 for materials used, process parameters, environmental and other conditions. Efficient, agile, flexible system To gain enhanced knowledge of product performance Increase manufacturing efficiency, reduce costs and over a range of material attributes, manufacturing project rejections and waste process options and process parameters considering Build scientific knowledge base for all products appropriate use of quality risk management principles.

9 8-10. Better interact with industry on science issues QbD BY PHARMACEUTICALS. Ensure consistent information Even though the pharmaceutical industry has focus on quality, it has failed to keep up with other industries in Incorporate risk management terms of manufacturing efficiency and productivity. 7-9. STEPS INVOLVED IN QUALITY BY DESIGN PRODUCTS Current scenario in the Pharmaceutical Industry: 1. Development of new molecular entity Cost of revalidation Preclinical study Off line analysis for in process need based Nonclinical study Product specifications as primary means of control Clinical Study Unpredictable Scale up issues Scale up Inability to understand failures Submission for market Approval Systematic approach to development: 2. Manufacturing That begins with predefined objectives Design Space Emphasizes products and process understanding Process Analytical Technology Process control (Figure 1).

10 Real time Quality Control International Journal of Pharmaceutical Sciences Review and Research Page 21. Available Online at Int. J. pharm . Sci. Rev. Res., 17(2), 2012; n 04, 20-28 ISSN 0976 044X. 12-14. CRITICAL QUALITY ATTRIBUTES. It is necessary to identify the quality attributes that are critical, those defining purity, potency and surrogate for Bioavailability Criticality etc. It is based on the impact of quality attribute/ parameter on the safety, efficacy & quality (manufacturability) of the Figure 1: Process, Quality, Design and PAT product. QUALITY TARGET PRODUCT PROFILE10,11 Establish a link between CPP & CQAs: Identification of attribute or parameters that can be used as a A summary of the drug development program described surrogate for clinical safety & efficacy (important to in terms of labeling concepts and it mainly focus on the patient) (Figure 2).