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