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Kazakhstan to undergo PIC/S on-site assessment in 2027

Regulatory Affairs TOP-Pharma Editorial Team -
Kazakhstan has been approved for an on-site assessment mission and an observed inspection in 2027 as part of its application for membership of the...

China’s revised medical device GMP takes effect, strengthening quality and contract manufacturing requirements

Medical Devices TOP-Pharma Editorial Team -
China’s National Medical Products Administration (NMPA) put its revised Good Manufacturing Practice (GMP) for Medical Devices into effect on 1 November 2026. Issued under...
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