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- W2186152676 abstract "Association of south East Asian nations (ASEAN) imitative to harmonize the requirements for drug registration is in progress and there will be single ASEAN market by 2015.ASEAN pharmaceutical market mostly depends on imports to meet the demand of health facilities and through development of ACTD they have provided a single window for drug approval in all 10 countries .therefore this review will try to focus on some main issues of the drug regulations throughout a very practical approach..A regulatory process, by which a person/organization /sponsor /innovator gets authorization to launch a drug in the market ,is known as drug approval process .every country has its own regulatory authority ,which is responsible to enforce the rules and regulations and disuse the guidelines to regulate the marketing of the drugs. This ASEAN common Technical Dossier (ACTD) is a guideline of the agreed upon common format for the preparation of a well-structured Common Technical Dossier (CTD) applications that will be submitted to ASEAN regulatory authorities for the registration of pharmaceuticals for the human use." @default.
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- W2186152676 date "2015-01-01" @default.
- W2186152676 modified "2023-09-26" @default.
- W2186152676 title "New Drug Approval Process In Singapore - A Detailed Dissertation For Registration of Multi - Source Drug Products" @default.
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