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