Activities involved in Computer Systems Validation
Activities involved in Computer Systems Validation
Computer Systems Validation (CSV)
is central to the life sciences industry. Apart from being a regulatory
requirement as set out by various regulatory authorities and practices such as
the FDA, EMA, GCP, GLP, GMP and all the Predicate Rules; CSV is also very
important to implement because not doing so will result in costly consequences.
More than anything else,
implementation of CSV is also important because it ensures that the data is
accurate and the information, secure. Implementing Computer Systems Validation
is also an important step in making sure that the organization restricts or
prevents any loss of revenue from its main activities or from the CSV exercise
itself. It also helps to thoroughly identify and close any gaps in the computer
systems.
Getting CSV is very important
With all these uses of a CSV; it
is imperative for life sciences organizations to understand how they can
implement a CSV that is effective and compliant with domestic and international
regulations. The CSV should ensure that the organization gets the most out of
it while meeting regulatory requirements.
A two day seminar from GlobalCompliancePanel, a premier brand of
NetZealous LLC, a well-known provider of professional trainings in the
regulatory compliance arena, will be of great value to regulatory professionals
who need to implement CSV. At this seminar, the highly regarded Angela Bazigos,
who is CEO of Touchstone Technologies Silicon Valley, Inc., will give a
complete understanding of the whole concept of Computer Systems Validation.
She will offer hands-on Understanding of the set of activities
involved in CSV, such as:
Just log on to http://globalcompliancepanel.viewpage.co/Validation-and-21-CFR-11-Compliance this site for more information.
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