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PharmaCompass offers a list of Aluminum stearate 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 Aluminum stearate manufacturer or Aluminum stearate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aluminum stearate manufacturer or Aluminum stearate supplier.
PharmaCompass also assists you with knowing the Aluminum stearate API Price utilized in the formulation of products. Aluminum stearate API Price is not always fixed or binding as the Aluminum stearate Price is obtained through a variety of data sources. The Aluminum stearate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ALUGEL 30DF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALUGEL 30DF, including repackagers and relabelers. The FDA regulates ALUGEL 30DF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALUGEL 30DF 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 ALUGEL 30DF manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALUGEL 30DF supplier is an individual or a company that provides ALUGEL 30DF active pharmaceutical ingredient (API) or ALUGEL 30DF finished formulations upon request. The ALUGEL 30DF suppliers may include ALUGEL 30DF API manufacturers, exporters, distributors and traders.
click here to find a list of ALUGEL 30DF suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ALUGEL 30DF DMF (Drug Master File) is a document detailing the whole manufacturing process of ALUGEL 30DF active pharmaceutical ingredient (API) in detail. Different forms of ALUGEL 30DF DMFs exist exist since differing nations have different regulations, such as ALUGEL 30DF USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ALUGEL 30DF DMF submitted to regulatory agencies in the US is known as a USDMF. ALUGEL 30DF USDMF includes data on ALUGEL 30DF's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ALUGEL 30DF USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ALUGEL 30DF suppliers with USDMF on PharmaCompass.
A ALUGEL 30DF CEP of the European Pharmacopoeia monograph is often referred to as a ALUGEL 30DF Certificate of Suitability (COS). The purpose of a ALUGEL 30DF CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ALUGEL 30DF EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ALUGEL 30DF to their clients by showing that a ALUGEL 30DF CEP has been issued for it. The manufacturer submits a ALUGEL 30DF CEP (COS) as part of the market authorization procedure, and it takes on the role of a ALUGEL 30DF CEP holder for the record. Additionally, the data presented in the ALUGEL 30DF CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ALUGEL 30DF DMF.
A ALUGEL 30DF CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ALUGEL 30DF 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 ALUGEL 30DF suppliers with CEP (COS) on PharmaCompass.
ALUGEL 30DF 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 ALUGEL 30DF 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 ALUGEL 30DF GMP manufacturer or ALUGEL 30DF GMP API supplier for your needs.
A ALUGEL 30DF CoA (Certificate of Analysis) is a formal document that attests to ALUGEL 30DF's compliance with ALUGEL 30DF specifications and serves as a tool for batch-level quality control.
ALUGEL 30DF CoA mostly includes findings from lab analyses of a specific batch. For each ALUGEL 30DF 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.
ALUGEL 30DF may be tested according to a variety of international standards, such as European Pharmacopoeia (ALUGEL 30DF EP), ALUGEL 30DF JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ALUGEL 30DF USP).
