The International Council for Harmonization (ICH) works to make global trade in the pharmaceutical industry easier. According to a recent article, the ICH “issued in December of 2017 a draft guidance aimed at more uniformity in rules on the quality of medicines throughout their lifecycles, particularly in the period after marketing authorization,” known as the Q12 guidelines. The guidelines, made available by the US Food and Drug Association (FDA) last May, are still in draft form and are in the process of undergoing public consultation through December 2018.
The goal of the Q12 guidelines is to cover lifecycle management issues not addressed in the ICH’s previous guidelines Q8-Q11. ICH Q12 covers the management of post-approval chemistry, manufacturing and controls (CMC) processes for both new and marketed drugs. Long term, the guidelines are predicted to reduce costs for regulators and manufacturers, as well as reduce variability and mitigate manufacturing, and quality shortages through the continual improvements on products says the FDA.
According to the Regulatory Affairs Professionals Society (RAPS), “Sections of the draft focus on the categorization of post-approval CMC changes, established conditions, post-approval change management protocols, product lifecycle management, pharmaceutical quality system and change management, the relationship between the regulatory assessment and inspection and post-approval changes for marketed products.”
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