Synopsis
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NDC API
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| Molecular Weight | 5040 g/mol |
|---|---|
| Molecular Formula | C215H358N72O66S |
| XLogP3 | -27.2 |
| Hydrogen Bond Donor Count | 83 |
| Hydrogen Bond Acceptor Count | 76 |
| Rotatable Bond Count | 183 |
| Exact Mass | 5038.6658354 g/mol |
| Monoisotopic Mass | 5036.6591258 g/mol |
| Topological Polar Surface Area | 2360 Ų |
| Heavy Atom Count | 354 |
| Formal Charge | 0 |
| Complexity | 12500 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 44 |
| 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 Growth Hormone-Releasing Hormone 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 Growth Hormone-Releasing Hormone manufacturer or Growth Hormone-Releasing Hormone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Growth Hormone-Releasing Hormone manufacturer or Growth Hormone-Releasing Hormone supplier.
PharmaCompass also assists you with knowing the Growth Hormone-Releasing Hormone API Price utilized in the formulation of products. Growth Hormone-Releasing Hormone API Price is not always fixed or binding as the Growth Hormone-Releasing Hormone Price is obtained through a variety of data sources. The Growth Hormone-Releasing Hormone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Somatocrinin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Somatocrinin, including repackagers and relabelers. The FDA regulates Somatocrinin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Somatocrinin 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 Somatocrinin supplier is an individual or a company that provides Somatocrinin active pharmaceutical ingredient (API) or Somatocrinin finished formulations upon request. The Somatocrinin suppliers may include Somatocrinin API manufacturers, exporters, distributors and traders.
click here to find a list of Somatocrinin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Somatocrinin DMF (Drug Master File) is a document detailing the whole manufacturing process of Somatocrinin active pharmaceutical ingredient (API) in detail. Different forms of Somatocrinin DMFs exist exist since differing nations have different regulations, such as Somatocrinin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Somatocrinin DMF submitted to regulatory agencies in the US is known as a USDMF. Somatocrinin USDMF includes data on Somatocrinin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Somatocrinin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Somatocrinin suppliers with USDMF on PharmaCompass.
Somatocrinin 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 Somatocrinin 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 Somatocrinin GMP manufacturer or Somatocrinin GMP API supplier for your needs.
A Somatocrinin CoA (Certificate of Analysis) is a formal document that attests to Somatocrinin's compliance with Somatocrinin specifications and serves as a tool for batch-level quality control.
Somatocrinin CoA mostly includes findings from lab analyses of a specific batch. For each Somatocrinin 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.
Somatocrinin may be tested according to a variety of international standards, such as European Pharmacopoeia (Somatocrinin EP), Somatocrinin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Somatocrinin USP).
