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1. Thorium X
1. Thorium X
2. 13233-32-4
3. 224ra
4. Radium, Isotope Of Mass 224
5. 5se5nog2nw
6. Radium-224 And Its Decay Products
7. Unii-5se5nog2nw
8. Radium Ra-224
9. Chebi:80503
10. Dtxsid50912341
Molecular Weight | 224.02021 g/mol |
---|---|
Molecular Formula | Ra |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 0 |
Rotatable Bond Count | 0 |
Exact Mass | 224.02021 g/mol |
Monoisotopic Mass | 224.02021 g/mol |
Topological Polar Surface Area | 0 Ų |
Heavy Atom Count | 1 |
Formal Charge | 0 |
Complexity | 0 |
Isotope Atom Count | 1 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Radium-224 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Radium-224, including repackagers and relabelers. The FDA regulates Radium-224 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Radium-224 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 Radium-224 supplier is an individual or a company that provides Radium-224 active pharmaceutical ingredient (API) or Radium-224 finished formulations upon request. The Radium-224 suppliers may include Radium-224 API manufacturers, exporters, distributors and traders.
click here to find a list of Radium-224 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Radium-224 DMF (Drug Master File) is a document detailing the whole manufacturing process of Radium-224 active pharmaceutical ingredient (API) in detail. Different forms of Radium-224 DMFs exist exist since differing nations have different regulations, such as Radium-224 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Radium-224 DMF submitted to regulatory agencies in the US is known as a USDMF. Radium-224 USDMF includes data on Radium-224's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Radium-224 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Radium-224 suppliers with USDMF on PharmaCompass.
Radium-224 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 Radium-224 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 Radium-224 GMP manufacturer or Radium-224 GMP API supplier for your needs.
A Radium-224 CoA (Certificate of Analysis) is a formal document that attests to Radium-224's compliance with Radium-224 specifications and serves as a tool for batch-level quality control.
Radium-224 CoA mostly includes findings from lab analyses of a specific batch. For each Radium-224 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.
Radium-224 may be tested according to a variety of international standards, such as European Pharmacopoeia (Radium-224 EP), Radium-224 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Radium-224 USP).
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