master file

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Noun1.master file - (computer science) a computer file that is used as the authority in a given job and that is relatively permanentmaster file - (computer science) a computer file that is used as the authority in a given job and that is relatively permanent
main file
computer science, computing - the branch of engineering science that studies (with the aid of computers) computable processes and structures
computer file - (computer science) a file maintained in computer-readable form
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In 2018, the global Electronic Trial Master File (eTMF) market size was million US$ and it is expected to reach million US$ by the end of 2025, with a CAGR of during 2019-2025.
Global Electronic Trial Master File (eTMF) Market 2019 Potential Growth, Share, Demand and Analysis of Market Challenges- Research Forecasts to 2025
Release date- 26082019 - Electronic Trial Master File (eTMF) Systems Market worth $1.8 billion by 2024.
Markets and markets-Electronic Trial Master File (eTMF) Systems Market worth $1.8 billion by 2024
Life science company Takara Bio USA Inc revealed on Thursday that it has submitted its Drug Master File to the US Food and Drug Administration (FDA) for the liquid formulation of RetroNectin GMP grade.
Takara Bio submits Drug Master File to FDA for RetroNectin GMP grade liquid format for development of cancer immunotherapies
Over the last few years, the electronic Trial Master File (eTMF) has been gaining widespread attention for integrating the TMF into a digital content platform.
Trial Master File: Paper or Electronic?
The turnover limit for reporting purposes is Rs50 million for the local file and Rs100 million for the Master File.
Pakistan aligns rules with oecd to curb tax evasion
For decades, certain advanced countries have established a system, drug master file (DMF), to provide confidential information applicable to APIs.[sup][1],[2] In general, a DMF contains the technical documents regarding chemistry, manufacturing, controls, packaging, and stability for an API.[sup][1],[2] In the United States, a DMF submission would not initiate the review process unless the new drug application (NDA) or abbreviated NDA (ANDA) is in relation to a specified DMF, where approval or disapproval of this DMF is not given.[sup][1]
Application profile of full and abbreviated dossiers for drug master file: An experience of Taiwan
Phlexglobal is a provider of Trial Master File solutions for global clinical trials, and has been central to the maturation of the TMF across the industry through participation in the creation of the TMF Reference Model.
Vitruvian Acquires Majority Shareholding in UK Trial Master File Solutions Firm Phlexglobal
* A master file of information relevant for all multinational company group members.
Understanding BEPS and the impact of country-by-country reporting
An FDA master file provides key information about the quality of components, materials and manufacturing processes used in producing medical devices and drugs, including related products such as biopreservation media used to preserve and store biologic materials including cells, tissues and organs.
FDA master files submitted for cell thawing media products
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