Synopsis
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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
A Growth Hormone-Releasing Hormone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Growth Hormone-Releasing Hormone, including repackagers and relabelers. The FDA regulates Growth Hormone-Releasing Hormone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Growth Hormone-Releasing Hormone 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 Growth Hormone-Releasing Hormone supplier is an individual or a company that provides Growth Hormone-Releasing Hormone active pharmaceutical ingredient (API) or Growth Hormone-Releasing Hormone finished formulations upon request. The Growth Hormone-Releasing Hormone suppliers may include Growth Hormone-Releasing Hormone API manufacturers, exporters, distributors and traders.
click here to find a list of Growth Hormone-Releasing Hormone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Growth Hormone-Releasing Hormone DMF (Drug Master File) is a document detailing the whole manufacturing process of Growth Hormone-Releasing Hormone active pharmaceutical ingredient (API) in detail. Different forms of Growth Hormone-Releasing Hormone DMFs exist exist since differing nations have different regulations, such as Growth Hormone-Releasing Hormone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Growth Hormone-Releasing Hormone DMF submitted to regulatory agencies in the US is known as a USDMF. Growth Hormone-Releasing Hormone USDMF includes data on Growth Hormone-Releasing Hormone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Growth Hormone-Releasing Hormone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Growth Hormone-Releasing Hormone suppliers with USDMF on PharmaCompass.
Growth Hormone-Releasing Hormone 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 Growth Hormone-Releasing Hormone 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 Growth Hormone-Releasing Hormone GMP manufacturer or Growth Hormone-Releasing Hormone GMP API supplier for your needs.
A Growth Hormone-Releasing Hormone CoA (Certificate of Analysis) is a formal document that attests to Growth Hormone-Releasing Hormone's compliance with Growth Hormone-Releasing Hormone specifications and serves as a tool for batch-level quality control.
Growth Hormone-Releasing Hormone CoA mostly includes findings from lab analyses of a specific batch. For each Growth Hormone-Releasing Hormone 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.
Growth Hormone-Releasing Hormone may be tested according to a variety of international standards, such as European Pharmacopoeia (Growth Hormone-Releasing Hormone EP), Growth Hormone-Releasing Hormone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Growth Hormone-Releasing Hormone USP).
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