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ABOUT THIS PAGE
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PharmaCompass offers a list of Sitafloxacin Hydrate 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 Sitafloxacin Hydrate manufacturer or Sitafloxacin Hydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sitafloxacin Hydrate manufacturer or Sitafloxacin Hydrate supplier.
PharmaCompass also assists you with knowing the Sitafloxacin Hydrate API Price utilized in the formulation of products. Sitafloxacin Hydrate API Price is not always fixed or binding as the Sitafloxacin Hydrate Price is obtained through a variety of data sources. The Sitafloxacin Hydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gracevit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gracevit, including repackagers and relabelers. The FDA regulates Gracevit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gracevit API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Gracevit manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gracevit supplier is an individual or a company that provides Gracevit active pharmaceutical ingredient (API) or Gracevit finished formulations upon request. The Gracevit suppliers may include Gracevit API manufacturers, exporters, distributors and traders.
click here to find a list of Gracevit suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gracevit DMF (Drug Master File) is a document detailing the whole manufacturing process of Gracevit active pharmaceutical ingredient (API) in detail. Different forms of Gracevit DMFs exist exist since differing nations have different regulations, such as Gracevit USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gracevit DMF submitted to regulatory agencies in the US is known as a USDMF. Gracevit USDMF includes data on Gracevit's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gracevit USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gracevit suppliers with USDMF 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 Gracevit Drug Master File in Japan (Gracevit JDMF) empowers Gracevit 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 Gracevit JDMF during the approval evaluation for pharmaceutical products. At the time of Gracevit 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 Gracevit suppliers with JDMF on PharmaCompass.
Gracevit 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 Gracevit 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 Gracevit GMP manufacturer or Gracevit GMP API supplier for your needs.
A Gracevit CoA (Certificate of Analysis) is a formal document that attests to Gracevit's compliance with Gracevit specifications and serves as a tool for batch-level quality control.
Gracevit CoA mostly includes findings from lab analyses of a specific batch. For each Gracevit 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.
Gracevit may be tested according to a variety of international standards, such as European Pharmacopoeia (Gracevit EP), Gracevit JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gracevit USP).
