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PharmaCompass offers a list of Carboxymethyl Cellulose 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 Carboxymethyl Cellulose manufacturer or Carboxymethyl Cellulose supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carboxymethyl Cellulose manufacturer or Carboxymethyl Cellulose supplier.
PharmaCompass also assists you with knowing the Carboxymethyl Cellulose API Price utilized in the formulation of products. Carboxymethyl Cellulose API Price is not always fixed or binding as the Carboxymethyl Cellulose Price is obtained through a variety of data sources. The Carboxymethyl Cellulose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Carmellose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carmellose, including repackagers and relabelers. The FDA regulates Carmellose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carmellose 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 Carmellose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carmellose supplier is an individual or a company that provides Carmellose active pharmaceutical ingredient (API) or Carmellose finished formulations upon request. The Carmellose suppliers may include Carmellose API manufacturers, exporters, distributors and traders.
click here to find a list of Carmellose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Carmellose DMF (Drug Master File) is a document detailing the whole manufacturing process of Carmellose active pharmaceutical ingredient (API) in detail. Different forms of Carmellose DMFs exist exist since differing nations have different regulations, such as Carmellose USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Carmellose DMF submitted to regulatory agencies in the US is known as a USDMF. Carmellose USDMF includes data on Carmellose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Carmellose USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Carmellose suppliers with USDMF on PharmaCompass.
Carmellose 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 Carmellose 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 Carmellose GMP manufacturer or Carmellose GMP API supplier for your needs.
A Carmellose CoA (Certificate of Analysis) is a formal document that attests to Carmellose's compliance with Carmellose specifications and serves as a tool for batch-level quality control.
Carmellose CoA mostly includes findings from lab analyses of a specific batch. For each Carmellose 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.
Carmellose may be tested according to a variety of international standards, such as European Pharmacopoeia (Carmellose EP), Carmellose JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Carmellose USP).
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