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