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API SUPPLIERS
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USDMF
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EUROAPI
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Rochem International Inc
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharm-RX Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pfanstiehl
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kirsch Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Dr. Paul Lohmann GmbH & Co. KGaA
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Actylis
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Aeon Procare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Bioplus Life Sciences
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Corel Pharma Chem
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Finar
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shijiazhuang Huaxu Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sigachi Industries
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Vasa Pharmachem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Zhejiang Huakang Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
12
PharmaCompass offers a list of Magnesium Carbonate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Magnesium Carbonate manufacturer or Magnesium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Carbonate manufacturer or Magnesium Carbonate supplier.
A Magfy manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magfy, including repackagers and relabelers. The FDA regulates Magfy manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magfy 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 Magfy manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Magfy supplier is an individual or a company that provides Magfy active pharmaceutical ingredient (API) or Magfy finished formulations upon request. The Magfy suppliers may include Magfy API manufacturers, exporters, distributors and traders.
click here to find a list of Magfy suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Magfy DMF (Drug Master File) is a document detailing the whole manufacturing process of Magfy active pharmaceutical ingredient (API) in detail. Different forms of Magfy DMFs exist exist since differing nations have different regulations, such as Magfy USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Magfy DMF submitted to regulatory agencies in the US is known as a USDMF. Magfy USDMF includes data on Magfy's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Magfy USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Magfy suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Magfy Drug Master File in Japan (Magfy JDMF) empowers Magfy API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Magfy JDMF during the approval evaluation for pharmaceutical products. At the time of Magfy JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Magfy suppliers with JDMF on PharmaCompass.
A Magfy CEP of the European Pharmacopoeia monograph is often referred to as a Magfy Certificate of Suitability (COS). The purpose of a Magfy CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Magfy EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Magfy to their clients by showing that a Magfy CEP has been issued for it. The manufacturer submits a Magfy CEP (COS) as part of the market authorization procedure, and it takes on the role of a Magfy CEP holder for the record. Additionally, the data presented in the Magfy CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Magfy DMF.
A Magfy CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Magfy CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Magfy suppliers with CEP (COS) on PharmaCompass.
A Magfy written confirmation (Magfy WC) is an official document issued by a regulatory agency to a Magfy manufacturer, verifying that the manufacturing facility of a Magfy active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Magfy APIs or Magfy finished pharmaceutical products to another nation, regulatory agencies frequently require a Magfy WC (written confirmation) as part of the regulatory process.
click here to find a list of Magfy 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 Magfy as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Magfy 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 Magfy 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 Magfy and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Magfy NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Magfy suppliers with NDC on PharmaCompass.
Magfy 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 Magfy GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Magfy GMP manufacturer or Magfy GMP API supplier for your needs.
A Magfy CoA (Certificate of Analysis) is a formal document that attests to Magfy's compliance with Magfy specifications and serves as a tool for batch-level quality control.
Magfy CoA mostly includes findings from lab analyses of a specific batch. For each Magfy 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.
Magfy may be tested according to a variety of international standards, such as European Pharmacopoeia (Magfy EP), Magfy JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Magfy USP).
