Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
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 pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deferiprone manufacturer or Deferiprone supplier.
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 CRMD-001 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CRMD-001, including repackagers and relabelers. The FDA regulates CRMD-001 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CRMD-001 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 CRMD-001 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CRMD-001 supplier is an individual or a company that provides CRMD-001 active pharmaceutical ingredient (API) or CRMD-001 finished formulations upon request. The CRMD-001 suppliers may include CRMD-001 API manufacturers, exporters, distributors and traders.
click here to find a list of CRMD-001 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CRMD-001 CEP of the European Pharmacopoeia monograph is often referred to as a CRMD-001 Certificate of Suitability (COS). The purpose of a CRMD-001 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CRMD-001 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CRMD-001 to their clients by showing that a CRMD-001 CEP has been issued for it. The manufacturer submits a CRMD-001 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CRMD-001 CEP holder for the record. Additionally, the data presented in the CRMD-001 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CRMD-001 DMF.
A CRMD-001 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CRMD-001 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 CRMD-001 suppliers with CEP (COS) on PharmaCompass.
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