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