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ABOUT THIS PAGE
A Gilteritinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gilteritinib, including repackagers and relabelers. The FDA regulates Gilteritinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gilteritinib API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Gilteritinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gilteritinib supplier is an individual or a company that provides Gilteritinib active pharmaceutical ingredient (API) or Gilteritinib finished formulations upon request. The Gilteritinib suppliers may include Gilteritinib API manufacturers, exporters, distributors and traders.
click here to find a list of Gilteritinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gilteritinib DMF (Drug Master File) is a document detailing the whole manufacturing process of Gilteritinib active pharmaceutical ingredient (API) in detail. Different forms of Gilteritinib DMFs exist exist since differing nations have different regulations, such as Gilteritinib USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gilteritinib DMF submitted to regulatory agencies in the US is known as a USDMF. Gilteritinib USDMF includes data on Gilteritinib's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gilteritinib USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gilteritinib suppliers with USDMF on PharmaCompass.
A Gilteritinib written confirmation (Gilteritinib WC) is an official document issued by a regulatory agency to a Gilteritinib manufacturer, verifying that the manufacturing facility of a Gilteritinib active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Gilteritinib APIs or Gilteritinib finished pharmaceutical products to another nation, regulatory agencies frequently require a Gilteritinib WC (written confirmation) as part of the regulatory process.
click here to find a list of Gilteritinib suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Gilteritinib as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Gilteritinib API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Gilteritinib as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Gilteritinib and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Gilteritinib NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Gilteritinib suppliers with NDC on PharmaCompass.
Gilteritinib Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Gilteritinib GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Gilteritinib GMP manufacturer or Gilteritinib GMP API supplier for your needs.
A Gilteritinib CoA (Certificate of Analysis) is a formal document that attests to Gilteritinib's compliance with Gilteritinib specifications and serves as a tool for batch-level quality control.
Gilteritinib CoA mostly includes findings from lab analyses of a specific batch. For each Gilteritinib CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Gilteritinib may be tested according to a variety of international standards, such as European Pharmacopoeia (Gilteritinib EP), Gilteritinib JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gilteritinib USP).
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