Synopsis
Synopsis
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CEP/COS
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JDMF
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| Molecular Weight | 6375 g/mol |
|---|---|
| Molecular Formula | C193H245N78O95P19S19 |
| XLogP3 | -8.3 |
| Hydrogen Bond Donor Count | 45 |
| Hydrogen Bond Acceptor Count | 146 |
| Rotatable Bond Count | 116 |
| Exact Mass | 6372.6513339 g/mol |
| Monoisotopic Mass | 6370.6446242 g/mol |
| Topological Polar Surface Area | 2860 A^2 |
| Heavy Atom Count | 404 |
| Formal Charge | 0 |
| Complexity | 18100 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 60 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Gti2040 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gti2040, including repackagers and relabelers. The FDA regulates Gti2040 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gti2040 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 Gti2040 supplier is an individual or a company that provides Gti2040 active pharmaceutical ingredient (API) or Gti2040 finished formulations upon request. The Gti2040 suppliers may include Gti2040 API manufacturers, exporters, distributors and traders.
click here to find a list of Gti2040 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gti2040 DMF (Drug Master File) is a document detailing the whole manufacturing process of Gti2040 active pharmaceutical ingredient (API) in detail. Different forms of Gti2040 DMFs exist exist since differing nations have different regulations, such as Gti2040 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gti2040 DMF submitted to regulatory agencies in the US is known as a USDMF. Gti2040 USDMF includes data on Gti2040's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gti2040 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gti2040 suppliers with USDMF on PharmaCompass.
Gti2040 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 Gti2040 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 Gti2040 GMP manufacturer or Gti2040 GMP API supplier for your needs.
A Gti2040 CoA (Certificate of Analysis) is a formal document that attests to Gti2040's compliance with Gti2040 specifications and serves as a tool for batch-level quality control.
Gti2040 CoA mostly includes findings from lab analyses of a specific batch. For each Gti2040 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.
Gti2040 may be tested according to a variety of international standards, such as European Pharmacopoeia (Gti2040 EP), Gti2040 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gti2040 USP).
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