01 1M/s. Vani Pharma Labs Ltd.,
01 1Propyphenazone (Ph. Eur.)
01 1WC-0188
01 1India
Date of Issue : 2019-09-17
Valid Till : 2022-09-16
Written Confirmation Number : WC-0188
Address of the Firm : 11 & 12, Indl. Development Area, Phase-I, Jeedimetla, Hyderabad-500 055, AP, Ind...
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PharmaCompass offers a list of Propyphenazone 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 Propyphenazone manufacturer or Propyphenazone supplier for your needs.
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PharmaCompass also assists you with knowing the Propyphenazone API Price utilized in the formulation of products. Propyphenazone API Price is not always fixed or binding as the Propyphenazone Price is obtained through a variety of data sources. The Propyphenazone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Demex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Demex, including repackagers and relabelers. The FDA regulates Demex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Demex 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 Demex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Demex supplier is an individual or a company that provides Demex active pharmaceutical ingredient (API) or Demex finished formulations upon request. The Demex suppliers may include Demex API manufacturers, exporters, distributors and traders.
click here to find a list of Demex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Demex written confirmation (Demex WC) is an official document issued by a regulatory agency to a Demex manufacturer, verifying that the manufacturing facility of a Demex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Demex APIs or Demex finished pharmaceutical products to another nation, regulatory agencies frequently require a Demex WC (written confirmation) as part of the regulatory process.
click here to find a list of Demex suppliers with Written Confirmation (WC) on PharmaCompass.
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