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International Journal of Pharmaceutical Investigation
Home»JPHI»Vol 6 Issue 3»Pharmaceutical Product Development: A Quality by Design Approach
Vol 6 Issue 3

Pharmaceutical Product Development: A Quality by Design Approach

August 1, 2016Updated:June 3, 20232 Mins Read
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International Journal of Pharmaceutical Investigation, 2016, 6, 3, 129-138.
DOI: 10.4103/2230-973X.187350
Published: August 2016
Type: Review Article

Authors: 

Kannissery Pramod
College of Pharmaceutical Sciences, Government Medical College, Kozhikode, Kerala, India.

M. Abu Tahir
Biogenero Labs Pvt Ltd., Unit No.1, Sy. No 179, C.K Palya, Hullahalli, Sakalvara Post, Bangalore, India.

Naseem A. Charoo
[3]Zayn Pharmaceuticals, Unit No. 2H-05-320, Floor No.5 Bldg No.2, Plot No. 550-554 J&G, DMCC, Dubai, United Arab Emirates; [4] AlFalah Life Sciences Pvt. Ltd. 27-Wathora, Budgam-191113, Jammu and Kashmir, India.

Shahid H. Ansari
Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

Javed Ali
Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

ABSTRACT

The application of quality by design (QbD) in pharmaceutical product development is now a thrust area for the regulatory authorities and the pharmaceutical industry. International Conference on Harmonization and United States Food and Drug Administration (USFDA) emphasized the principles and applications of QbD in pharmaceutical development in their guidance for the industry. QbD attributes are addressed in question-based review, developed by USFDA for chemistry, manufacturing, and controls section of abbreviated new drug applications. QbD principles, when implemented, lead to a successful product development, subsequent prompt regulatory approval, reduce exhaustive validation burden, and significantly reduce post-approval changes. The key elements of QbD viz., target product quality profile, critical quality attributes, risk assessments, design space, control strategy, product lifecycle management, and continual improvement are discussed to understand the performance of dosage forms within design space. Design of experiments, risk assessment tools, and process analytical technology are also discussed for their role in QbD. This review underlines the importance of QbD in inculcating science-based approach in pharmaceutical product development.

Keywords: Design of experiments, Design space, Process analytical technology, Risk assessment, Quality by Design, QbD .

Review Article
Previous ArticleImproved Dissolution and Anti-inflammatory Activity of Ibuprofen-polyethylene Glycol 8000 Solid Dispersion Systems
Next Article Development, Evaluation and Influence of Formulation and Process Variables on In vitro Performance of Oral Elementary Osmotic Device of Atenolol

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