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1. R 1507
2. R-1507
3. R-1507 Monoclonal Antibody
4. R1507
5. Ro-4858696
6. Ro-4858696-000
7. Ro-4858696000
8. Ro4858696
9. Ro4858696-000
10. Rv-001
11. Rv001
12. Tepezza
13. Teprotumumab
14. Teprotumumab-trbw
1. Onilcamotide [inn]
2. Unii-uqe6kp7t0d
3. Uqe6kp7t0d
4. Rhoc Peptide Vaccine Rv001v
5. Rv001
6. Rv-001
7. Ala-thr-arg-ala-gly-leu-gln-val-arg-lys-asn-lys-arg-arg-arg-gly-cys-pro-ile-leu
8. 1164096-85-8
9. L-alanyl-l-threonyl-l-arginyl-l-alanylglycyl-l-leucyl-l-glutaminyl-l-valyl-l-arginyl-l-lysyl-l-asparaginyl-l-lysyl-l-arginyl-l-arginyl-l-arginylglycyl-l-cysteinyl-l-prolyl-l-isoleucyl-l-leucine
10. L-leucine, L-alanyl-l-threonyl-l-arginyl-l-alanylglycyl-l-leucyl-l-glutaminyl-l-valyl-l-arginyl-l-lysyl-l-asparaginyl-l-lysyl-l-arginyl-l-arginyl-l-arginylglycyl-l-cysteinyl-l-prolyl-l-isoleucyl-
| Molecular Weight | 2293.7 g/mol |
|---|---|
| Molecular Formula | C96H177N39O24S |
| XLogP3 | -11.3 |
| Hydrogen Bond Donor Count | 41 |
| Hydrogen Bond Acceptor Count | 33 |
| Rotatable Bond Count | 85 |
| Exact Mass | 2293.3582937 g/mol |
| Monoisotopic Mass | 2292.3549388 g/mol |
| Topological Polar Surface Area | 1080 Ų |
| Heavy Atom Count | 160 |
| Formal Charge | 0 |
| Complexity | 4890 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 20 |
| 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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A RV001 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RV001, including repackagers and relabelers. The FDA regulates RV001 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RV001 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 RV001 supplier is an individual or a company that provides RV001 active pharmaceutical ingredient (API) or RV001 finished formulations upon request. The RV001 suppliers may include RV001 API manufacturers, exporters, distributors and traders.
RV001 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 RV001 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 RV001 GMP manufacturer or RV001 GMP API supplier for your needs.
A RV001 CoA (Certificate of Analysis) is a formal document that attests to RV001's compliance with RV001 specifications and serves as a tool for batch-level quality control.
RV001 CoA mostly includes findings from lab analyses of a specific batch. For each RV001 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.
RV001 may be tested according to a variety of international standards, such as European Pharmacopoeia (RV001 EP), RV001 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (RV001 USP).
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