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INTERNATIONAL JOURNAL OF CREATIVE RESEARCH THOUGHTS - IJCRT (IJCRT.ORG)
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STUDY ON DMF FILLING IN CONTEXT TO US, EUROPE, JAPAN AND ITS COMPARISON
Authors
Shaikh Mohammad shahzeb
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Keywords
drug master file, active substance master file, master file, eCTD, marketing authorization, API, USFDA, EMA, PMDA
Abstract
This is a collection of documents that provide full and accurate information on an active pharmaceutical ingredient (API) or a final medicinal dosage form in the pharmaceutical industry. It is now referred to as an active substance master file as a result of the European drug master file (ASMF). All prescription and over-the-counter medications in the United States are listed in a single database. The chemistry, manufacturing, stability, purity, and cGMP status of any human pharmaceutical product are all recorded in a drug master file (DMF) (DMF). In order to get an investigational new drug, new drug, or abbreviated new drug application, a DMF is required to meet regulatory standards and establish the medical product's quality, safety, and efficacy. To acquire market authorization, the drug master file must be structured and content differ from that of Europe (MA). To support regulatory requirements, the primary objective is to establish the product's quality, safety, and efficacy. A pharmaceutical company has created and presented this paper to the target market. There is no need to submit a DMF since there is no regulatory obligation. Confidential information concerning facilities, procedures, and products utilized in the production and processing of one or more human medicines is provided to the regulatory authority in this document. When two or more companies collaborate on the development or production of a drug product, a DMF is filed. Companies may safeguard their intellectual property by registering DMFs while still meeting regulatory disclosure requirements for processing information A drug master file was compiled in a variety of ways across the US, Europe, and Japan, according to the findings. Drug master files administered by the Food and Drug Administration (USA), Japan's PMDA, and the European Medicines Agency (EMA) are also included (EMA). In order to submit a drug master file in the US, Japan, and Europe, you need this information. As a result of this research, you will have a better understanding of how to fill out a drug master file in the nations stated above, as well as what the differences are between the countries. The DMF primarily supports regulatory requirements pertaining to the proof of quality, safety, and effectiveness in order to help secure a pharmaceutical product's marketing authorization. To keep up with the latest regulatory submissions, this research examined new updates and revisions to the drug master file according to the eCTD or electronic format utilized by most regulated nations as of 2016.
IJCRT's Publication Details
Unique Identification Number - IJCRT2203221
Paper ID - 216596
Author type - Indian Author
Page Number(s) - b916-b956
Pubished in - Volume 10 | Issue 3 | March 2022
DOI (Digital Object Identifier) -
No Of Downloads - 487
Author Country - India, 431401, parbhani, parbhani, 431401, Pharmacy All
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Shaikh Mohammad shahzeb, "STUDY ON DMF FILLING IN CONTEXT TO US, EUROPE, JAPAN AND ITS COMPARISON", International Journal of Creative Research Thoughts (IJCRT), ISSN:2320-2882, Volume.10, Issue 3, pp.b916-b956, March 2022, Available at :http://www.ijcrt.org/papers/IJCRT2203221.pdf
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