ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): Kaustubh Jagtap, Bharati Chaudhari, Vivekkumar Redasani

Email(s): kaustubhjagtap121@gmail.com

DOI: 10.52711/0974-4150.2022.00054   

Address: Kaustubh Jagtap*, Bharati Chaudhari, Vivekkumar Redasani YSPM’s Yashoda Technical Campus, Faculty of Pharmacy, Satara, 415003. *Corresponding Author E-mail:

Published In:   Volume - 15,      Issue - 4,     Year - 2022


ABSTRACT:
Quality by Design (QbD) refers to a holistic approach towards drug development. Quality by design is a vital part of the modern approach to pharmaceutical quality. The purpose of this practice school topic is to discuss the pharmaceutical Quality by Design (QbD) and illustrate how it can be used to ensure pharmaceutical quality. The QbD is a systemic approach to pharmaceutical development. It means designing and developing formulations and manufacturing processes to ensure predefined product quality. Some of the QbD elements include: Defining Quality target product profile, identifying critical quality attributes, link the drug excipients attributes, establishing design space, control strategy, critical process parameters and product life cycle management. Using QbD, pharmaceutical quality is assured by understanding and controlling formulation and manufacturing variables. A new approach to drug development could increase efficiencies, provide regulatory support and flexibility, and offer important business benefits throughout the product’s life cycle. This PS topic explores the processes used in developing a market formulation and required supportive data, particularly in light of the industry’s current movement toward submissions based on QbD. The work also facilitates the adoption and implementation of QbD. Principles in the development of pharmaceutical industries. Successful implementation of QbD concepts requires cooperation across a multitude of company teams, from R&D to manufacturing to quality control and regulatory affairs. This is necessary to ensure that QbD concepts are incorporated not only when the first activities are initiated around a product’s design but also during the design of the process used to make the product and other activities associated with a product’s life cycle. The application of the concept of quality by design (QbD) presented in this paper aligns with the principles of ICH Q8, Q9 and Q10 guidelines.


Cite this article:
Kaustubh Jagtap, Bharati Chaudhari, Vivekkumar Redasani. Quality by Design (QbD) concept Review in Pharmaceuticals. Asian Journal of Research in Chemistry. 2022; 15(4):303-7. doi: 10.52711/0974-4150.2022.00054

Cite(Electronic):
Kaustubh Jagtap, Bharati Chaudhari, Vivekkumar Redasani. Quality by Design (QbD) concept Review in Pharmaceuticals. Asian Journal of Research in Chemistry. 2022; 15(4):303-7. doi: 10.52711/0974-4150.2022.00054   Available on: https://www.ajrconline.org/AbstractView.aspx?PID=2022-15-4-11


REFERENCE:
1.    Hardik Patel, Shraddha Parmar, Bhavna Patel, Int. J. Pharm. Sci. Rev. Res., 21(1), Jul – Aug 2013. 223-235.
2.    Audumbar Mali, Santosh Jadhav, Ashpak Tamboli, Gorakhnath Hake, Inventi Rapid: Pharmaceutical Process Development Vol. 2015, 1.
3.    Woodcock J, The concept of pharmaceutical quality. American Pharmaceutical Review, 7(6), 2004, 10–15. 11. 4. J.M. Juran, A. B. Godfrey, Juran’s Quality Handbook, 5th Edition, McGraw-Hill, 1998, 29.1
4.    Nishendu P. Nadpara, Rakshit V. Thumar, Vidhi N. Kalola, Parul B. Patel, Int. J. Pharm. Sci. Rev. Res., 17(2), 2012, 20-21.
5.    Akash Mali, Monali Jagtap, Poonam Karekar, Audrius Maruska, International Journal of Pharmaceutical Research, 2016, 11-14.
6.    Q10: Pharmaceutical Quality System, ICH Tripartite Guidelines. International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human.
7.    FDA Guidance for Industry and Review Staff: Target Product Profile – A Strategic Development Process Tool (Draft Guidance).
8.    Q8 (R1): Pharmaceutical Development, Revision 1, ICH Harmonized Tripartite Guidelines, International Conference on Harmonization of Technical.
9.    Sachin L. Darkunde, International Journal of Pharmaceutical Chemistry and Analysis, January- March,2018;5(1):1-6
10.    Nally J.D, Bunn G, Good Manufacturing Practice for Pharmaceuticals, Sixth Edition, 169, 2007, 352.
11.    National Institute for Pharmaceutical Technology and Education. Strategic Roadmap for Research and Education, http://www. nipte.org, 2006, 33.
12.    Gibson M, Product optimization, In M. Gibson (ed.), Pharmaceutical Preformulation and Formulation, Taylor and Francis, New York, 2001, 295-330nalytical Chemistry, 59, 1987, 624A–637A.
13.    Lionberger RA, Lee LS, Lee L, Raw A, Yu LX, Quality by design: Concepts for ANDAs, The AAPS Journal, 10, 2008, 268–276.
14.    Roy S (2012) “Quality by Design-Holistic concept of concept of building quality in pharmaceuticals”. Int. J Pham Biomed Res 3:100-108.

Recomonded Articles:

Author(s): Ravi N. Patel, Urviben Y. Patel, Kiran M. Patel, Jimit S. Patel, Ankit D. Patel, Dhrubo Jyoti Sen

DOI:         Access: Open Access Read More

Author(s): Chavan Pooja Ajit, Avinash Mahadeo Bhagwat, Atul Prabhakar Chaudhari

DOI: 10.52711/0974-4150.2021.00061         Access: Open Access Read More

Author(s): Y. Padmavathi, Akari Anjali, Nayaka Raghavendra Babu, P Ravi Kumar

DOI: 10.5958/0974-4150.2017.00064.5         Access: Open Access Read More

Author(s): Nachiket S. Dighe, Priyanka R. Varade, Ganesh S. Shinde, Priya S. Rao

DOI: 10.5958/0974-4150.2019.00028.2         Access: Open Access Read More

Author(s): PA Jadhav, CS Raut, JP Bidada, BB Buwa, PN Dhabale, SC Dhawale

DOI:         Access: Open Access Read More

Author(s): Alka Verma, Bhupesh Verma, Sunil Kumar Prajapati, Kishu Tripathi

DOI:         Access: Open Access Read More

Author(s): Vatchavai Bhaskara Raju, Bonthu Mohan Gandhi, Kamatham Srinivas Sumanth, Kolli Srinivas, Tupakula N Venkata Lakshmi Neeraja

DOI: 10.5958/0974-4150.2017.00030.X         Access: Open Access Read More

Author(s): Banerjee S, Bonde CG, Merukar SS, Patil YR

DOI:         Access: Open Access Read More

Author(s): Nikita N. Patel, Charmy S. Kothari

DOI:         Access: Open Access Read More

Author(s): Shashi Ravi Suman Rudrangi, Vijaya Kumar Bontha, Venkata Reddy Manda, Srinivas Bethi

DOI:         Access: Open Access Read More

Asian Journal of Research in Chemistry (AJRC) is an international, peer-reviewed journal devoted to pure and applied chemistry..... Read more >>>

RNI: Not Available                     
DOI: 10.5958/0974-4150 

Popular Articles


Recent Articles




Tags