Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
02 1KATWIJK CHEMIE BV Katwijk ZH NL
01 2Deferiprone
01 1India
02 1Netherlands
01 2Valid
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : CEP 2024-124 - Rev 00
Status : Valid
Issue Date : 2024-10-09
Type : Chemical
Substance Number : 2236
Certificate Number : R0-CEP 2020-354 - Rev 00
Status : Valid
Issue Date : 2022-04-19
Type : Chemical
Substance Number : 2236
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PharmaCompass offers a list of Deferiprone 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 Deferiprone manufacturer or Deferiprone supplier for your needs.
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PharmaCompass also assists you with knowing the Deferiprone API Price utilized in the formulation of products. Deferiprone API Price is not always fixed or binding as the Deferiprone Price is obtained through a variety of data sources. The Deferiprone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BP-12415 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BP-12415, including repackagers and relabelers. The FDA regulates BP-12415 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BP-12415 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A BP-12415 supplier is an individual or a company that provides BP-12415 active pharmaceutical ingredient (API) or BP-12415 finished formulations upon request. The BP-12415 suppliers may include BP-12415 API manufacturers, exporters, distributors and traders.
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A BP-12415 CEP of the European Pharmacopoeia monograph is often referred to as a BP-12415 Certificate of Suitability (COS). The purpose of a BP-12415 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of BP-12415 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of BP-12415 to their clients by showing that a BP-12415 CEP has been issued for it. The manufacturer submits a BP-12415 CEP (COS) as part of the market authorization procedure, and it takes on the role of a BP-12415 CEP holder for the record. Additionally, the data presented in the BP-12415 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the BP-12415 DMF.
A BP-12415 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. BP-12415 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 BP-12415 suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering BP-12415
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