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