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PharmaCompass offers a list of Valsartan 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 Valsartan manufacturer or Valsartan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Valsartan manufacturer or Valsartan supplier.
PharmaCompass also assists you with knowing the Valsartan API Price utilized in the formulation of products. Valsartan API Price is not always fixed or binding as the Valsartan Price is obtained through a variety of data sources. The Valsartan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Valsartan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Valsartan, including repackagers and relabelers. The FDA regulates Valsartan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Valsartan 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 Valsartan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Valsartan supplier is an individual or a company that provides Valsartan active pharmaceutical ingredient (API) or Valsartan finished formulations upon request. The Valsartan suppliers may include Valsartan API manufacturers, exporters, distributors and traders.
click here to find a list of Valsartan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Valsartan DMF (Drug Master File) is a document detailing the whole manufacturing process of Valsartan active pharmaceutical ingredient (API) in detail. Different forms of Valsartan DMFs exist exist since differing nations have different regulations, such as Valsartan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Valsartan DMF submitted to regulatory agencies in the US is known as a USDMF. Valsartan USDMF includes data on Valsartan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Valsartan USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Valsartan 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 Valsartan Drug Master File in Japan (Valsartan JDMF) empowers Valsartan 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 Valsartan JDMF during the approval evaluation for pharmaceutical products. At the time of Valsartan 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 Valsartan suppliers with JDMF 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 Valsartan Drug Master File in Korea (Valsartan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Valsartan. The MFDS reviews the Valsartan KDMF as part of the drug registration process and uses the information provided in the Valsartan KDMF to evaluate the safety and efficacy of the drug.
After submitting a Valsartan 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 Valsartan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Valsartan suppliers with KDMF on PharmaCompass.
A Valsartan CEP of the European Pharmacopoeia monograph is often referred to as a Valsartan Certificate of Suitability (COS). The purpose of a Valsartan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Valsartan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Valsartan to their clients by showing that a Valsartan CEP has been issued for it. The manufacturer submits a Valsartan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Valsartan CEP holder for the record. Additionally, the data presented in the Valsartan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Valsartan DMF.
A Valsartan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Valsartan 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 Valsartan suppliers with CEP (COS) on PharmaCompass.
A Valsartan written confirmation (Valsartan WC) is an official document issued by a regulatory agency to a Valsartan manufacturer, verifying that the manufacturing facility of a Valsartan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Valsartan APIs or Valsartan finished pharmaceutical products to another nation, regulatory agencies frequently require a Valsartan WC (written confirmation) as part of the regulatory process.
click here to find a list of Valsartan suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Valsartan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Valsartan API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Valsartan as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Valsartan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Valsartan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Valsartan suppliers with NDC on PharmaCompass.
Valsartan 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 Valsartan 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 Valsartan GMP manufacturer or Valsartan GMP API supplier for your needs.
A Valsartan CoA (Certificate of Analysis) is a formal document that attests to Valsartan's compliance with Valsartan specifications and serves as a tool for batch-level quality control.
Valsartan CoA mostly includes findings from lab analyses of a specific batch. For each Valsartan 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.
Valsartan may be tested according to a variety of international standards, such as European Pharmacopoeia (Valsartan EP), Valsartan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Valsartan USP).
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