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