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01 1GE HEALTHCARE AS Oslo NO
02 1ROTEM INDUSTRIES LTD. Dimona IL
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01 2Tetra-O-acetyl-mannose triflate for radiopharmaceutical preparations
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01 1Israel
02 1United Kingdom
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01 2Valid
Tetra-O-acetyl-mannose Triflate For Radiopharmac...
Certificate Number : CEP 2022-176 - Rev 00
Status : Valid
Issue Date : 2024-02-20
Type : Chemical
Substance Number : 2294
Tetra-O-acetyl-mannose Triflate For Radiopharmac...
Certificate Number : CEP 2011-287 - Rev 03
Status : Valid
Issue Date : 2025-01-14
Type : Chemical
Substance Number : 2294
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PharmaCompass offers a list of TATM 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 TATM manufacturer or TATM supplier for your needs.
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PharmaCompass also assists you with knowing the TATM API Price utilized in the formulation of products. TATM API Price is not always fixed or binding as the TATM Price is obtained through a variety of data sources. The TATM Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 92051-23-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 92051-23-5, including repackagers and relabelers. The FDA regulates 92051-23-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 92051-23-5 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A 92051-23-5 supplier is an individual or a company that provides 92051-23-5 active pharmaceutical ingredient (API) or 92051-23-5 finished formulations upon request. The 92051-23-5 suppliers may include 92051-23-5 API manufacturers, exporters, distributors and traders.
click here to find a list of 92051-23-5 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 92051-23-5 CEP of the European Pharmacopoeia monograph is often referred to as a 92051-23-5 Certificate of Suitability (COS). The purpose of a 92051-23-5 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 92051-23-5 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 92051-23-5 to their clients by showing that a 92051-23-5 CEP has been issued for it. The manufacturer submits a 92051-23-5 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 92051-23-5 CEP holder for the record. Additionally, the data presented in the 92051-23-5 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 92051-23-5 DMF.
A 92051-23-5 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 92051-23-5 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 92051-23-5 suppliers with CEP (COS) on PharmaCompass.
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