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