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Τι (ποιος) είναι inventory master file - ορισμός

DOCUMENT IN THE PHARMACEUTICAL INDUSTRY

Active Substance Master File; US-Drug Master file

Inventory valuation

ACCOUNTING METHODS USED IN DETERMINING THE VALUE OF INVENTORY

Beginning Inventory; Inventory Costing; Inventory costing; Inventory valuation adjustment; Inventory cost

An inventory valuation allows a company to provide a monetary value for items that make up their inventory. Inventories are usually the largest current asset of a business, and proper measurement of them is necessary to assure accurate financial statements.

https://en.wikipedia.org/wiki/Inventory_valuation

Inventory theory

MATHEMATICAL STUDY CONCERNED WITH THE DESIGN OF INVENTORY SYSTEMS

Inventory control problem; Inventory model; Inventory models

Material theory (or more formally the mathematical theory of inventory and production) is the sub-specialty within operations research and operations management that is concerned with the design of production/inventory systems to minimize costs: it studies the decisions faced by firms and the military in connection with manufacturing, warehousing, supply chains, spare part allocation and so on and provides the mathematical foundation for logistics. The inventory control problem is the problem faced by a firm that must decide how much to order in each time period to meet demand for its products.

https://en.wikipedia.org/wiki/Inventory_theory

Inventory turnover

MEASURE OF THE NUMBER OF TIMES INVENTORY IS SOLD OR USED IN A TIME PERIOD

Inventory turns; Inventory Turns; Turnover ratio; Inventory Turnover; Inventory turnover ratio; Stock turnover

In accounting, the inventory turnover is a measure of the number of times inventory is sold or used in a time period such as a year. It is calculated to see if a business has an excessive inventory in comparison to its sales level.

https://en.wikipedia.org/wiki/Inventory_turnover

Βικιπαίδεια

Drug Master File

Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market. There is no regulatory requirement to file a DMF. However, the document provides the regulatory authority with confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs. Typically, a drug master file is filed when two or more firms work in partnership on developing or manufacturing a drug product. The DMF filing allows a firm to protect its intellectual property from its partner while complying with regulatory requirements for disclosure of processing details.

https://en.wikipedia.org/wiki/Drug Master File