Synopsis
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CEP/COS
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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Health Canada Patents
US Medicaid
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Regulatory FDF Prices
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
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...
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...
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PharmaCompass offers a list of Exatecan 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 Exatecan manufacturer or Exatecan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Exatecan manufacturer or Exatecan supplier.
PharmaCompass also assists you with knowing the Exatecan API Price utilized in the formulation of products. Exatecan API Price is not always fixed or binding as the Exatecan Price is obtained through a variety of data sources. The Exatecan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Exatecan Mesylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Exatecan Mesylate, including repackagers and relabelers. The FDA regulates Exatecan Mesylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Exatecan Mesylate 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 Exatecan Mesylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Exatecan Mesylate supplier is an individual or a company that provides Exatecan Mesylate active pharmaceutical ingredient (API) or Exatecan Mesylate finished formulations upon request. The Exatecan Mesylate suppliers may include Exatecan Mesylate API manufacturers, exporters, distributors and traders.
click here to find a list of Exatecan Mesylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Exatecan Mesylate DMF (Drug Master File) is a document detailing the whole manufacturing process of Exatecan Mesylate active pharmaceutical ingredient (API) in detail. Different forms of Exatecan Mesylate DMFs exist exist since differing nations have different regulations, such as Exatecan Mesylate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Exatecan Mesylate DMF submitted to regulatory agencies in the US is known as a USDMF. Exatecan Mesylate USDMF includes data on Exatecan Mesylate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Exatecan Mesylate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Exatecan Mesylate suppliers with USDMF on PharmaCompass.
Exatecan Mesylate 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 Exatecan Mesylate 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 Exatecan Mesylate GMP manufacturer or Exatecan Mesylate GMP API supplier for your needs.
A Exatecan Mesylate CoA (Certificate of Analysis) is a formal document that attests to Exatecan Mesylate's compliance with Exatecan Mesylate specifications and serves as a tool for batch-level quality control.
Exatecan Mesylate CoA mostly includes findings from lab analyses of a specific batch. For each Exatecan Mesylate 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.
Exatecan Mesylate may be tested according to a variety of international standards, such as European Pharmacopoeia (Exatecan Mesylate EP), Exatecan Mesylate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Exatecan Mesylate USP).
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