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