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01 1VITAL LABORATORIES PVT. LIMITED Mumbai IN
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01 1Reserpine
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01 1India
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01 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R0-CEP 2010-041 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2011-11-29
Type : Chemical
Substance Number : 528
34
PharmaCompass offers a list of Reserpine 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 Reserpine manufacturer or Reserpine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Reserpine manufacturer or Reserpine supplier.
PharmaCompass also assists you with knowing the Reserpine API Price utilized in the formulation of products. Reserpine API Price is not always fixed or binding as the Reserpine Price is obtained through a variety of data sources. The Reserpine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LS-1306 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LS-1306, including repackagers and relabelers. The FDA regulates LS-1306 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LS-1306 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 LS-1306 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LS-1306 supplier is an individual or a company that provides LS-1306 active pharmaceutical ingredient (API) or LS-1306 finished formulations upon request. The LS-1306 suppliers may include LS-1306 API manufacturers, exporters, distributors and traders.
click here to find a list of LS-1306 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LS-1306 CEP of the European Pharmacopoeia monograph is often referred to as a LS-1306 Certificate of Suitability (COS). The purpose of a LS-1306 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LS-1306 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LS-1306 to their clients by showing that a LS-1306 CEP has been issued for it. The manufacturer submits a LS-1306 CEP (COS) as part of the market authorization procedure, and it takes on the role of a LS-1306 CEP holder for the record. Additionally, the data presented in the LS-1306 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LS-1306 DMF.
A LS-1306 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LS-1306 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of LS-1306 suppliers with CEP (COS) on PharmaCompass.
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