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Molecular Weight | 1670.8 g/mol |
---|---|
Molecular Formula | C74H115N19O25 |
XLogP3 | -7.2 |
Hydrogen Bond Donor Count | 26 |
Hydrogen Bond Acceptor Count | 42 |
Rotatable Bond Count | 62 |
Exact Mass | 1669.83115023 g/mol |
Monoisotopic Mass | 1669.83115023 g/mol |
Topological Polar Surface Area | 801 Ų |
Heavy Atom Count | 118 |
Formal Charge | 0 |
Complexity | 3540 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 12 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Global Sales Information
ABOUT THIS PAGE
A Interferon Beta(103-115)[Human] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Interferon Beta(103-115)[Human], including repackagers and relabelers. The FDA regulates Interferon Beta(103-115)[Human] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Interferon Beta(103-115)[Human] 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 Interferon Beta(103-115)[Human] supplier is an individual or a company that provides Interferon Beta(103-115)[Human] active pharmaceutical ingredient (API) or Interferon Beta(103-115)[Human] finished formulations upon request. The Interferon Beta(103-115)[Human] suppliers may include Interferon Beta(103-115)[Human] API manufacturers, exporters, distributors and traders.
Interferon Beta(103-115)[Human] 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 Interferon Beta(103-115)[Human] 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 Interferon Beta(103-115)[Human] GMP manufacturer or Interferon Beta(103-115)[Human] GMP API supplier for your needs.
A Interferon Beta(103-115)[Human] CoA (Certificate of Analysis) is a formal document that attests to Interferon Beta(103-115)[Human]'s compliance with Interferon Beta(103-115)[Human] specifications and serves as a tool for batch-level quality control.
Interferon Beta(103-115)[Human] CoA mostly includes findings from lab analyses of a specific batch. For each Interferon Beta(103-115)[Human] 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.
Interferon Beta(103-115)[Human] may be tested according to a variety of international standards, such as European Pharmacopoeia (Interferon Beta(103-115)[Human] EP), Interferon Beta(103-115)[Human] JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Interferon Beta(103-115)[Human] USP).
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