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PharmaCompass offers a list of Radium-223 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 Radium-223 manufacturer or Radium-223 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Radium-223 manufacturer or Radium-223 supplier.
PharmaCompass also assists you with knowing the Radium-223 API Price utilized in the formulation of products. Radium-223 API Price is not always fixed or binding as the Radium-223 Price is obtained through a variety of data sources. The Radium-223 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A XOFIGO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of XOFIGO, including repackagers and relabelers. The FDA regulates XOFIGO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. XOFIGO 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 XOFIGO supplier is an individual or a company that provides XOFIGO active pharmaceutical ingredient (API) or XOFIGO finished formulations upon request. The XOFIGO suppliers may include XOFIGO API manufacturers, exporters, distributors and traders.
XOFIGO 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 XOFIGO 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 XOFIGO GMP manufacturer or XOFIGO GMP API supplier for your needs.
A XOFIGO CoA (Certificate of Analysis) is a formal document that attests to XOFIGO's compliance with XOFIGO specifications and serves as a tool for batch-level quality control.
XOFIGO CoA mostly includes findings from lab analyses of a specific batch. For each XOFIGO 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.
XOFIGO may be tested according to a variety of international standards, such as European Pharmacopoeia (XOFIGO EP), XOFIGO JP (Japanese Pharmacopeia) and the US Pharmacopoeia (XOFIGO USP).
