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1. 186re Radioisotope
2. Re-186 Radioisotope
1. Rhenium Re-186
2. Zu7f1et6tm
3. 14998-63-1
4. (~186~re)rhenium
5. Unii-zu7f1et6tm
6. 186re
7. Rhenium (186-re)
8. Rhenium, Isotope Of Mass 186
9. Dtxsid60933825
10. Rhenium-186 [who-dd]
11. Q18882928
| Molecular Weight | 185.954989 g/mol |
|---|---|
| Molecular Formula | Re |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 185.954989 g/mol |
| Monoisotopic Mass | 185.954989 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 |
Drugs in Development
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ABOUT THIS PAGE
A Rhenium-186 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rhenium-186, including repackagers and relabelers. The FDA regulates Rhenium-186 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rhenium-186 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 Rhenium-186 supplier is an individual or a company that provides Rhenium-186 active pharmaceutical ingredient (API) or Rhenium-186 finished formulations upon request. The Rhenium-186 suppliers may include Rhenium-186 API manufacturers, exporters, distributors and traders.
Rhenium-186 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 Rhenium-186 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 Rhenium-186 GMP manufacturer or Rhenium-186 GMP API supplier for your needs.
A Rhenium-186 CoA (Certificate of Analysis) is a formal document that attests to Rhenium-186's compliance with Rhenium-186 specifications and serves as a tool for batch-level quality control.
Rhenium-186 CoA mostly includes findings from lab analyses of a specific batch. For each Rhenium-186 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.
Rhenium-186 may be tested according to a variety of international standards, such as European Pharmacopoeia (Rhenium-186 EP), Rhenium-186 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rhenium-186 USP).
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