What Is Computer System Validation (CSV) and Why It’s Crucial for Compliance
Introduction Definition of Computer System Validation (CSV). Computer System Validation (CSV) is the process of ensuring that computer systems and software used in regulated environments consistently produce accurate, reliable, and compliant results. This involves a series of documented activities that confirm the system meets its intended purpose and complies with relevant regulations and standards. CSV […]
USFDA 483 on Access Management of Computerized System
Observation  1. Your firm failed to exercise appropriate controls over computer or related systems to assure that only authorized personnel institute changes in master production and control records, or other records (21 CFR 211.68(b)). Your firm manufactures over-the-counter (OTC) drug products, including alcohol-based hand sanitizers[1]. During the inspection of your facility, our investigator attempted […]
Top online institutes to get your “Computer system Validation training & certification”
Our annual ranking on Computer System Validation (CSV) training institute aims to highlight the best providers of CSV training in India and Outside of India. The ranking is concluded after an in-depth analysis and a detailed process of vetting through various training institutes in India, US, Ireland, China and Rest of the word. We reached […]
Category Of Software & Hardware As Per GAMP Guideline & their Validation
Category of software Application are categorized into following software categories as per GAMP 5 guideline 1. Category 1 – Infrastructure Software:- There are two types of software in this category: A. Commercially available layered software: – Software upon which applications are built or applications are developed to run under the control of this kind of […]
Computer Software Assurance: New Way of Computerized System Validation
Now a days everyone is shifting from CSV to CSA, a risk based and more efficient validation approach as compared to generating piles of documents which is un-necessary, only to satisfy regulatory bodies. However regulatory bodies does not want to generate piles of documents for validating computerized system rather than they want companies to have […]