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API SUPPLIERS
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
Sumar Biotech work together to Innovate & Manufacture Semi-synthetic, Synthetic & Fermentation API.
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Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
About the Company : Headquartered in Fengxian District, Shanghai Minbiotech Co., Ltd. is a company specializing in the R&D and production of advanced pharmaceutical intermediates and biological API...
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
About the Company : Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product gro...
Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
About the Company : Omgene Life Sciences Private Limited is an R&D-driven biopharmaceutical company specializing in biopharmaceuticals, peptides, semi-synthetic, and synthetic actives. As a vertically...
Sumar Biotech work together to Innovate & Manufacture Semi-synthetic, Synthetic & Fermentation API.
About the Company : Sumar Biotech LLP, registered in January 2018, is a startup approved by the Gujarat State Biotechnology Mission. It was founded by emerging entrepreneurs and a team of young yet ex...
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PharmaCompass offers a list of Rezafungin 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 Rezafungin manufacturer or Rezafungin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rezafungin manufacturer or Rezafungin supplier.
PharmaCompass also assists you with knowing the Rezafungin API Price utilized in the formulation of products. Rezafungin API Price is not always fixed or binding as the Rezafungin Price is obtained through a variety of data sources. The Rezafungin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rezafungin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rezafungin, including repackagers and relabelers. The FDA regulates Rezafungin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rezafungin 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 Rezafungin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rezafungin supplier is an individual or a company that provides Rezafungin active pharmaceutical ingredient (API) or Rezafungin finished formulations upon request. The Rezafungin suppliers may include Rezafungin API manufacturers, exporters, distributors and traders.
click here to find a list of Rezafungin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Rezafungin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Rezafungin 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 Rezafungin 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 Rezafungin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Rezafungin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Rezafungin suppliers with NDC on PharmaCompass.
Rezafungin 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 Rezafungin 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 Rezafungin GMP manufacturer or Rezafungin GMP API supplier for your needs.
A Rezafungin CoA (Certificate of Analysis) is a formal document that attests to Rezafungin's compliance with Rezafungin specifications and serves as a tool for batch-level quality control.
Rezafungin CoA mostly includes findings from lab analyses of a specific batch. For each Rezafungin 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.
Rezafungin may be tested according to a variety of international standards, such as European Pharmacopoeia (Rezafungin EP), Rezafungin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rezafungin USP).
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