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PharmaCompass offers a list of Ethanol 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 Ethanol manufacturer or Ethanol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethanol manufacturer or Ethanol supplier.
PharmaCompass also assists you with knowing the Ethanol API Price utilized in the formulation of products. Ethanol API Price is not always fixed or binding as the Ethanol Price is obtained through a variety of data sources. The Ethanol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 02882_SIAL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 02882_SIAL, including repackagers and relabelers. The FDA regulates 02882_SIAL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 02882_SIAL 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 02882_SIAL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 02882_SIAL supplier is an individual or a company that provides 02882_SIAL active pharmaceutical ingredient (API) or 02882_SIAL finished formulations upon request. The 02882_SIAL suppliers may include 02882_SIAL API manufacturers, exporters, distributors and traders.
click here to find a list of 02882_SIAL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 02882_SIAL DMF (Drug Master File) is a document detailing the whole manufacturing process of 02882_SIAL active pharmaceutical ingredient (API) in detail. Different forms of 02882_SIAL DMFs exist exist since differing nations have different regulations, such as 02882_SIAL USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 02882_SIAL DMF submitted to regulatory agencies in the US is known as a USDMF. 02882_SIAL USDMF includes data on 02882_SIAL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 02882_SIAL USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 02882_SIAL 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 02882_SIAL Drug Master File in Japan (02882_SIAL JDMF) empowers 02882_SIAL 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 02882_SIAL JDMF during the approval evaluation for pharmaceutical products. At the time of 02882_SIAL 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 02882_SIAL suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 02882_SIAL Drug Master File in Korea (02882_SIAL KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 02882_SIAL. The MFDS reviews the 02882_SIAL KDMF as part of the drug registration process and uses the information provided in the 02882_SIAL KDMF to evaluate the safety and efficacy of the drug.
After submitting a 02882_SIAL KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their 02882_SIAL API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 02882_SIAL suppliers with KDMF on PharmaCompass.
A 02882_SIAL CEP of the European Pharmacopoeia monograph is often referred to as a 02882_SIAL Certificate of Suitability (COS). The purpose of a 02882_SIAL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 02882_SIAL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 02882_SIAL to their clients by showing that a 02882_SIAL CEP has been issued for it. The manufacturer submits a 02882_SIAL CEP (COS) as part of the market authorization procedure, and it takes on the role of a 02882_SIAL CEP holder for the record. Additionally, the data presented in the 02882_SIAL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 02882_SIAL DMF.
A 02882_SIAL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 02882_SIAL 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 02882_SIAL suppliers with CEP (COS) on PharmaCompass.
02882_SIAL 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 02882_SIAL 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 02882_SIAL GMP manufacturer or 02882_SIAL GMP API supplier for your needs.
A 02882_SIAL CoA (Certificate of Analysis) is a formal document that attests to 02882_SIAL's compliance with 02882_SIAL specifications and serves as a tool for batch-level quality control.
02882_SIAL CoA mostly includes findings from lab analyses of a specific batch. For each 02882_SIAL 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.
02882_SIAL may be tested according to a variety of international standards, such as European Pharmacopoeia (02882_SIAL EP), 02882_SIAL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (02882_SIAL USP).