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1. 15702-53-1
2. Ccris 3941
3. Magnesium Silicate (mg3si2o7)
4. Dtxsid40166194
| Molecular Weight | 149.00 g/mol |
|---|---|
| Molecular Formula | Mg3O3Si+4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 147.9167955 g/mol |
| Monoisotopic Mass | 147.9167955 g/mol |
| Topological Polar Surface Area | 63.2 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 4 |
| Complexity | 18.8 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 4 |
ABOUT THIS PAGE
A CCRIS 3941 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCRIS 3941, including repackagers and relabelers. The FDA regulates CCRIS 3941 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCRIS 3941 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 CCRIS 3941 supplier is an individual or a company that provides CCRIS 3941 active pharmaceutical ingredient (API) or CCRIS 3941 finished formulations upon request. The CCRIS 3941 suppliers may include CCRIS 3941 API manufacturers, exporters, distributors and traders.
click here to find a list of CCRIS 3941 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The CCRIS 3941 Drug Master File in Japan (CCRIS 3941 JDMF) empowers CCRIS 3941 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the CCRIS 3941 JDMF during the approval evaluation for pharmaceutical products. At the time of CCRIS 3941 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of CCRIS 3941 suppliers with JDMF on PharmaCompass.
CCRIS 3941 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 CCRIS 3941 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 CCRIS 3941 GMP manufacturer or CCRIS 3941 GMP API supplier for your needs.
A CCRIS 3941 CoA (Certificate of Analysis) is a formal document that attests to CCRIS 3941's compliance with CCRIS 3941 specifications and serves as a tool for batch-level quality control.
CCRIS 3941 CoA mostly includes findings from lab analyses of a specific batch. For each CCRIS 3941 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.
CCRIS 3941 may be tested according to a variety of international standards, such as European Pharmacopoeia (CCRIS 3941 EP), CCRIS 3941 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CCRIS 3941 USP).
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