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