Be it in the pharmaceutical or medical device industry, any minor deviation either in the processes or in data maintenance, could easily trigger regulatory warnings and product recalls. The consequences are huge in terms of time, money, resources, and much more. In such regulated environments, organizations must comply to industry regulations when it comes to assuring to data integrity, or risk suffering huge, yet preventable consequences. This white paper helps understand why the regulated industry must ensure data accuracy, and how data completeness allows organizations to breathe easy. It also highlights how ill-treatment of data will disrupt organizations' chances to meet Current Good Manufacturing Practices (cGMPs) or Good Laboratory Practices (GLP). Finally, the white paper discloses how technological solutions help in implementing a holistic approach to data integrity.

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