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