The importance of data integrity in the Pharma industry




Data integrity is the accuracy and validity of data that exists even after its life. For enterprises that depend on these data, they are mainly expected to be precise and reliable. Then, there’s always the risk of losing sensitive data or data manipulation. This is the main reason that data integrity solutions play a major role in the security of enterprises. 
When talking about security, data integrity can be compromised in many ways. Transfer of data might result in altered or removed information. This is where data integrity software comes into play to monitor data integrity issues. The software needs to support 21 CFR Part 11 compliance. This ensures compatibility with multiple platforms of different servers and browsers. 
Maintaining proper data integrity is important for any organization, especially in the pharma biotech sector. Making sure that the data produced is accurate and consistent not only helps in an efficient internal process, but also helps the organization to avoid any legal issues in data integrity pharma. When we take the pharma industry into account, a lot of warning letters have been issued by the FDA (US Food and Drug Administration) since its incorporation of data integrity objectives in 2010. This resulted in companies struggling to comply with the FDA regulations when it came to data errors, incomplete records, missing documents and inappropriate manual integration. ALCOA Data Integrity 
There are different causes for data integrity issues in pharma. Some of the major causes include ignorance, human error and inefficient systems. It’s important that standard procedures are easy to navigate that don’t allow data integrity breaches to slip out. The core structure of Agaram Tech’s data integrity assurance system is based on ALCOA principle. This principle ensures that the data is attributable, legible, contemporaneous, original and accurate. For more info visit Alcoa Data Integrity

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