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PharmaCompass offers a list of Thymine 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 Thymine manufacturer or Thymine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Thymine manufacturer or Thymine supplier.
PharmaCompass also assists you with knowing the Thymine API Price utilized in the formulation of products. Thymine API Price is not always fixed or binding as the Thymine Price is obtained through a variety of data sources. The Thymine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Thymine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thymine, including repackagers and relabelers. The FDA regulates Thymine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thymine 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 Thymine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Thymine supplier is an individual or a company that provides Thymine active pharmaceutical ingredient (API) or Thymine finished formulations upon request. The Thymine suppliers may include Thymine API manufacturers, exporters, distributors and traders.
click here to find a list of Thymine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Thymine 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 Thymine 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 Thymine GMP manufacturer or Thymine GMP API supplier for your needs.
A Thymine CoA (Certificate of Analysis) is a formal document that attests to Thymine's compliance with Thymine specifications and serves as a tool for batch-level quality control.
Thymine CoA mostly includes findings from lab analyses of a specific batch. For each Thymine 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.
Thymine may be tested according to a variety of international standards, such as European Pharmacopoeia (Thymine EP), Thymine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Thymine USP).