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PharmaCompass offers a list of Meldonium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Meldonium manufacturer or Meldonium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Meldonium manufacturer or Meldonium supplier.
PharmaCompass also assists you with knowing the Meldonium API Price utilized in the formulation of products. Meldonium API Price is not always fixed or binding as the Meldonium Price is obtained through a variety of data sources. The Meldonium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mildronate dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mildronate dihydrate, including repackagers and relabelers. The FDA regulates Mildronate dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mildronate dihydrate 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 Mildronate dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mildronate dihydrate supplier is an individual or a company that provides Mildronate dihydrate active pharmaceutical ingredient (API) or Mildronate dihydrate finished formulations upon request. The Mildronate dihydrate suppliers may include Mildronate dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Mildronate dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mildronate dihydrate CEP of the European Pharmacopoeia monograph is often referred to as a Mildronate dihydrate Certificate of Suitability (COS). The purpose of a Mildronate dihydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mildronate dihydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mildronate dihydrate to their clients by showing that a Mildronate dihydrate CEP has been issued for it. The manufacturer submits a Mildronate dihydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mildronate dihydrate CEP holder for the record. Additionally, the data presented in the Mildronate dihydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mildronate dihydrate DMF.
A Mildronate dihydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mildronate dihydrate 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 Mildronate dihydrate suppliers with CEP (COS) on PharmaCompass.
A Mildronate dihydrate written confirmation (Mildronate dihydrate WC) is an official document issued by a regulatory agency to a Mildronate dihydrate manufacturer, verifying that the manufacturing facility of a Mildronate dihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Mildronate dihydrate APIs or Mildronate dihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Mildronate dihydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Mildronate dihydrate suppliers with Written Confirmation (WC) on PharmaCompass.
Mildronate dihydrate 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 Mildronate dihydrate 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 Mildronate dihydrate GMP manufacturer or Mildronate dihydrate GMP API supplier for your needs.
A Mildronate dihydrate CoA (Certificate of Analysis) is a formal document that attests to Mildronate dihydrate's compliance with Mildronate dihydrate specifications and serves as a tool for batch-level quality control.
Mildronate dihydrate CoA mostly includes findings from lab analyses of a specific batch. For each Mildronate dihydrate 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.
Mildronate dihydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Mildronate dihydrate EP), Mildronate dihydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mildronate dihydrate USP).
