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PharmaCompass offers a list of 1190-53-0 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 1190-53-0 manufacturer or 1190-53-0 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 1190-53-0 manufacturer or 1190-53-0 supplier.
PharmaCompass also assists you with knowing the 1190-53-0 API Price utilized in the formulation of products. 1190-53-0 API Price is not always fixed or binding as the 1190-53-0 Price is obtained through a variety of data sources. The 1190-53-0 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-801-899 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-801-899, including repackagers and relabelers. The FDA regulates MolPort-001-801-899 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-801-899 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 MolPort-001-801-899 supplier is an individual or a company that provides MolPort-001-801-899 active pharmaceutical ingredient (API) or MolPort-001-801-899 finished formulations upon request. The MolPort-001-801-899 suppliers may include MolPort-001-801-899 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-801-899 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 MolPort-001-801-899 Drug Master File in Japan (MolPort-001-801-899 JDMF) empowers MolPort-001-801-899 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 MolPort-001-801-899 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-801-899 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 MolPort-001-801-899 suppliers with JDMF on PharmaCompass.
MolPort-001-801-899 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 MolPort-001-801-899 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 MolPort-001-801-899 GMP manufacturer or MolPort-001-801-899 GMP API supplier for your needs.
A MolPort-001-801-899 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-801-899's compliance with MolPort-001-801-899 specifications and serves as a tool for batch-level quality control.
MolPort-001-801-899 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-801-899 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.
MolPort-001-801-899 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-801-899 EP), MolPort-001-801-899 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-801-899 USP).