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