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