Author(s): Yogita Chowdhary, Babita kumar

Email(s): Yogitachowdhary85@gmail.com

DOI: 10.52711/2231-5675.2023.00010   

Address: Yogita Chowdhary, Babita kumar
Sanskar College of Pharmacy and Research, Ghaziabad - 201001.
*Corresponding Author

Published In:   Volume - 13,      Issue - 1,     Year - 2023


ABSTRACT:
Change Control is the process that management uses to identify, document and authorize changes to an IT environment. It minimizes the likelihood of disruptions, unauthorized alterations and errors. The change control procedures should be designed with the size and complexity of the environment in mind. Change control is used to ensure changes to a product or system are introduced in a controlled and coordinated manner. It reduces the possibility that unnecessary changes will be introduced to a system without forethought, introducing faults into the system or undoing changes made by other users of software. The goals of a change control procedure usually include minimal disruption to services, reduction in back-out activities, and cost-effective utilization of resources involved in implementing change. Change control is used in various industries, including in IT, software development, the pharmaceutical industry, the medical device industry, and other engineering/manufacturing industries. For the IT and software industries, change control is a major aspect of the broader discipline of change management. There are two types of changes 1. Disruptive change 2. Dynamic change. is a non-localized future irreversible and change that affects a portion of an industry. This can be caused by changes in market trends causing a shift in the mode of production to fit the customer demands. Dynamic Change is multi-dimensional change that is predictable on a measurable scale. Change control is a CGMP concept that focuses on managing change to prevent unintended consequences. Manufacturing changes (i.e changes that alter specifications, a critical product attribute or bioavailability) require regulatory filings and prior regulatory approval.


Cite this article:
Yogita Chowdhary, Babita kumar. Importance of Change control in Pharmaceutical Industry: A Review. Asian Journal of Pharmaceutical Analysis. 2023; 13(1):59-0. doi: 10.52711/2231-5675.2023.00010

Cite(Electronic):
Yogita Chowdhary, Babita kumar. Importance of Change control in Pharmaceutical Industry: A Review. Asian Journal of Pharmaceutical Analysis. 2023; 13(1):59-0. doi: 10.52711/2231-5675.2023.00010   Available on: https://ajpaonline.com/AbstractView.aspx?PID=2023-13-1-10


REFERENCE:
1.    Matteson, S. (7 July 2017). "10 essential elements of change control management". TechRepublic. CBS Interactive, Inc. Retrieved 20 May 2018.
2.    Hall, P.A.V.; Ramil, J.C.F. (2007). Managing the Software Enterprise: Software Engineering and Information Systems in Context. Cengage Learning. pp. 318–325. Retrieved 20 May 2018.
3.    Turner, S.G. (15 December 2003). Pharmaceutical Engineering Change Control. Taylor and Francis. pp. 200.
4.    Teixeira, M.B. (2013). Design Controls for the Medical Device Industry (2nd ed.). CRC Press. p. 205.
5.    Monahanm E. (1995). Engineering Documentation Control Practices & Procedures. CRC Press. p. 280.
6.    Herzig, T.W.; Walsh, T.; Gallagher, L.A. (2013). Implementing Information Security in Healthcare: Building a Security Program. Healthcare Information and Management Systems Society. pp. 204–205.

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