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1. Human Insulin, Solution
| Molecular Weight | 5808 g/mol |
|---|---|
| Molecular Formula | C257H383N65O77S6 |
| XLogP3 | -13.1 |
| Hydrogen Bond Donor Count | 78 |
| Hydrogen Bond Acceptor Count | 89 |
| Rotatable Bond Count | 179 |
| Exact Mass | 5805.6443599 g/mol |
| Monoisotopic Mass | 5803.6376502 g/mol |
| Topological Polar Surface Area | 2450 Ų |
| Heavy Atom Count | 405 |
| Formal Charge | 0 |
| Complexity | 14600 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 52 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Velosiline Hm 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 Velosiline Hm manufacturer or Velosiline Hm supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Velosiline Hm manufacturer or Velosiline Hm supplier.
PharmaCompass also assists you with knowing the Velosiline Hm API Price utilized in the formulation of products. Velosiline Hm API Price is not always fixed or binding as the Velosiline Hm Price is obtained through a variety of data sources. The Velosiline Hm Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Velosiline Hm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Velosiline Hm, including repackagers and relabelers. The FDA regulates Velosiline Hm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Velosiline Hm 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 Velosiline Hm supplier is an individual or a company that provides Velosiline Hm active pharmaceutical ingredient (API) or Velosiline Hm finished formulations upon request. The Velosiline Hm suppliers may include Velosiline Hm API manufacturers, exporters, distributors and traders.
Velosiline Hm 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 Velosiline Hm 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 Velosiline Hm GMP manufacturer or Velosiline Hm GMP API supplier for your needs.
A Velosiline Hm CoA (Certificate of Analysis) is a formal document that attests to Velosiline Hm's compliance with Velosiline Hm specifications and serves as a tool for batch-level quality control.
Velosiline Hm CoA mostly includes findings from lab analyses of a specific batch. For each Velosiline Hm 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.
Velosiline Hm may be tested according to a variety of international standards, such as European Pharmacopoeia (Velosiline Hm EP), Velosiline Hm JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Velosiline Hm USP).
