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GLP- Good Laboratory Practice.
In August 2016, the FDA published�and is currently reviewing�a revised
set of proposed Good Laboratory Practices (GLP) regulations.
They are currently conducting surveillance inspections of laboratories, testing
sites, and CROs to ensure that facilities comply with GLP and can maintain data
integrity for their studies. If a Study Director
does not have the ability to ensure both GLP compliance and data integrity,
they can be subject to a Form 483, other Warning Letters, and more. The essential advantage of following current Good Laboratory Practice is
the making of an archive trail giving detectability to all estimations. This
prompts the making of in fact defendable logical information, by which its
quality, dependability, and reliability can be guaranteed.
Benefits of GLP Certifications