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PharmaCompass offers a list of Glyceryl Stearate 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 Glyceryl Stearate manufacturer or Glyceryl Stearate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glyceryl Stearate manufacturer or Glyceryl Stearate supplier.
PharmaCompass also assists you with knowing the Glyceryl Stearate API Price utilized in the formulation of products. Glyceryl Stearate API Price is not always fixed or binding as the Glyceryl Stearate Price is obtained through a variety of data sources. The Glyceryl Stearate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1379-EP2270006A1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1379-EP2270006A1, including repackagers and relabelers. The FDA regulates 1379-EP2270006A1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1379-EP2270006A1 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 1379-EP2270006A1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1379-EP2270006A1 supplier is an individual or a company that provides 1379-EP2270006A1 active pharmaceutical ingredient (API) or 1379-EP2270006A1 finished formulations upon request. The 1379-EP2270006A1 suppliers may include 1379-EP2270006A1 API manufacturers, exporters, distributors and traders.
click here to find a list of 1379-EP2270006A1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1379-EP2270006A1 DMF (Drug Master File) is a document detailing the whole manufacturing process of 1379-EP2270006A1 active pharmaceutical ingredient (API) in detail. Different forms of 1379-EP2270006A1 DMFs exist exist since differing nations have different regulations, such as 1379-EP2270006A1 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1379-EP2270006A1 DMF submitted to regulatory agencies in the US is known as a USDMF. 1379-EP2270006A1 USDMF includes data on 1379-EP2270006A1's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1379-EP2270006A1 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1379-EP2270006A1 suppliers with USDMF on PharmaCompass.
1379-EP2270006A1 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 1379-EP2270006A1 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 1379-EP2270006A1 GMP manufacturer or 1379-EP2270006A1 GMP API supplier for your needs.
A 1379-EP2270006A1 CoA (Certificate of Analysis) is a formal document that attests to 1379-EP2270006A1's compliance with 1379-EP2270006A1 specifications and serves as a tool for batch-level quality control.
1379-EP2270006A1 CoA mostly includes findings from lab analyses of a specific batch. For each 1379-EP2270006A1 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.
1379-EP2270006A1 may be tested according to a variety of international standards, such as European Pharmacopoeia (1379-EP2270006A1 EP), 1379-EP2270006A1 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1379-EP2270006A1 USP).
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