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