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Registration Of Drug Product In Malaysia 2025

In Malaysia, drug product registration is regulated by the National Pharmaceutical Regulatory Agency (NPRA) under the Ministry of Health Malaysia (MOH). All pharmaceutical products intended for importation, manufacture, distribution, or sale must be registered with the NPRA to ensure their safety, efficacy, and quality...

Registration Of Drug Product In Phillippines 2025

In the Philippines, the registration of a drug product is regulated by the Food and Drug Administration (FDA Philippines) under the Department of Health (DOH). The registration process requires submission of a comprehensive dossier in the ASEAN Common Technical Dossier (ACTD) format, organized into four main parts...

Registration Of Drug Product In Singapore 2025

In Singapore, the registration of drug products is regulated by the Health Sciences Authority (HSA), under the Ministry of Health. The process requires submission of a Common Technical Document (CTD)-formatted dossier, comprising Modules 1 to 5 or ACTD format. Module 1 contains Singapore-specific administrative...

Registration Of Drug Product In Vietnam 2025

In Vietnam, the registration of a drug product is regulated by the Drug Administration of Vietnam (DAV), under the Ministry of Health (MOH).The registration process requires submission of a comprehensive dossier in the ASEAN Common Technical Dossier (ACTD) format, organized into four main parts (Parts I to IV), covering...

Registration Of Drug Product In Myanmar 2025

In Myanmar, drug product registration is regulated by the Food and Drug Administration (FDA Myanmar) under the Ministry of Health. All pharmaceutical products intended for import, manufacture, or sale in Myanmar must be registered with FDA Myanmar to ensure safety, efficacy, and quality. The registration process requires...