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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 Aluminium stearate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminium stearate, including repackagers and relabelers. The FDA regulates Aluminium stearate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminium stearate 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 Aluminium stearate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aluminium stearate supplier is an individual or a company that provides Aluminium stearate active pharmaceutical ingredient (API) or Aluminium stearate finished formulations upon request. The Aluminium stearate suppliers may include Aluminium stearate API manufacturers, exporters, distributors and traders.
click here to find a list of Aluminium stearate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aluminium stearate DMF (Drug Master File) is a document detailing the whole manufacturing process of Aluminium stearate active pharmaceutical ingredient (API) in detail. Different forms of Aluminium stearate DMFs exist exist since differing nations have different regulations, such as Aluminium stearate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aluminium stearate DMF submitted to regulatory agencies in the US is known as a USDMF. Aluminium stearate USDMF includes data on Aluminium stearate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aluminium stearate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Aluminium stearate suppliers with USDMF on PharmaCompass.
A Aluminium stearate CEP of the European Pharmacopoeia monograph is often referred to as a Aluminium stearate Certificate of Suitability (COS). The purpose of a Aluminium stearate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aluminium stearate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aluminium stearate to their clients by showing that a Aluminium stearate CEP has been issued for it. The manufacturer submits a Aluminium stearate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aluminium stearate CEP holder for the record. Additionally, the data presented in the Aluminium stearate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aluminium stearate DMF.
A Aluminium stearate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aluminium stearate 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 Aluminium stearate suppliers with CEP (COS) on PharmaCompass.
Aluminium stearate 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 Aluminium stearate 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 Aluminium stearate GMP manufacturer or Aluminium stearate GMP API supplier for your needs.
A Aluminium stearate CoA (Certificate of Analysis) is a formal document that attests to Aluminium stearate's compliance with Aluminium stearate specifications and serves as a tool for batch-level quality control.
Aluminium stearate CoA mostly includes findings from lab analyses of a specific batch. For each Aluminium stearate 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.
Aluminium stearate may be tested according to a variety of international standards, such as European Pharmacopoeia (Aluminium stearate EP), Aluminium stearate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aluminium stearate USP).
