กองยากองยาhttps://drug.fda.moph.go.thth12610EU Variation Guidelinehttps://drug.fda.moph.go.th/gen-km/km-08/Fri, 31 Jan 25 14:38:00 +0700ASEAN Variation Guideline for Pharmaceutical producthttps://drug.fda.moph.go.th/gen-km/km-07/Fri, 31 Jan 25 14:36:56 +0700ASEAN Guideline for the Conduct of Bioavailability and Bioequivalence Studieshttps://drug.fda.moph.go.th/gen-km/km-06/Fri, 31 Jan 25 14:35:46 +0700ASEAN Guideline on Stability Study of Drug Producthttps://drug.fda.moph.go.th/gen-km/km-05/Fri, 31 Jan 25 14:34:58 +0700ASEAN Guideline for Validation of Analytical Procedureshttps://drug.fda.moph.go.th/gen-km/km-04/Fri, 31 Jan 25 14:34:03 +0700ASEAN Guideline on Submission of Manufacturing Process Validation Data for Drug Registrationhttps://drug.fda.moph.go.th/gen-km/km-03/Fri, 31 Jan 25 14:30:44 +0700ICHhttps://drug.fda.moph.go.th/gen-km/km-26/Tue, 28 Jan 25 14:44:00 +0700IPRP Working Groupshttps://drug.fda.moph.go.th/gen-km/km-25/Tue, 28 Jan 25 14:43:00 +0700Denmark Published RMPhttps://drug.fda.moph.go.th/gen-km/km-24/Tue, 28 Jan 25 14:41:00 +0700Health Canadahttps://drug.fda.moph.go.th/gen-km/km-23/Tue, 28 Jan 25 14:38:00 +0700