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API SUPPLIERS
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EU WC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
About the Company : Established in 2012, Nuray Chemicals Pvt Ltd is an API manufacturer for highly regulated markets. Its manufacturing facility with state-of-the-art R&D is located near Chennai in th...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
About the Company : Cohance Lifesciences is a leading CDMO and API platform, offering products and services across all phases of a molecule’s lifecycle from development to commercialzation. With our...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Global Sales Information
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PharmaCompass offers a list of Brivudine 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 Brivudine manufacturer or Brivudine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Brivudine manufacturer or Brivudine supplier.
PharmaCompass also assists you with knowing the Brivudine API Price utilized in the formulation of products. Brivudine API Price is not always fixed or binding as the Brivudine Price is obtained through a variety of data sources. The Brivudine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zostex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zostex, including repackagers and relabelers. The FDA regulates Zostex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zostex 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 Zostex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zostex supplier is an individual or a company that provides Zostex active pharmaceutical ingredient (API) or Zostex finished formulations upon request. The Zostex suppliers may include Zostex API manufacturers, exporters, distributors and traders.
click here to find a list of Zostex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zostex written confirmation (Zostex WC) is an official document issued by a regulatory agency to a Zostex manufacturer, verifying that the manufacturing facility of a Zostex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zostex APIs or Zostex finished pharmaceutical products to another nation, regulatory agencies frequently require a Zostex WC (written confirmation) as part of the regulatory process.
click here to find a list of Zostex suppliers with Written Confirmation (WC) on PharmaCompass.
Zostex 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 Zostex 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 Zostex GMP manufacturer or Zostex GMP API supplier for your needs.
A Zostex CoA (Certificate of Analysis) is a formal document that attests to Zostex's compliance with Zostex specifications and serves as a tool for batch-level quality control.
Zostex CoA mostly includes findings from lab analyses of a specific batch. For each Zostex 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.
Zostex may be tested according to a variety of international standards, such as European Pharmacopoeia (Zostex EP), Zostex JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zostex USP).
