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