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01 GE HEALTHCARE AS Oslo NO (1)
02 ROTEM INDUSTRIES LTD. Dimona IL (1)
01 Tetra-O-acetyl-mannose triflate for radiopharmaceutical preparations (2)
01 Israel (1)
02 United Kingdom (1)
01 Valid (2)
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred TATM manufacturer or TATM supplier.
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 TATM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TATM, including repackagers and relabelers. The FDA regulates TATM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TATM 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 TATM supplier is an individual or a company that provides TATM active pharmaceutical ingredient (API) or TATM finished formulations upon request. The TATM suppliers may include TATM API manufacturers, exporters, distributors and traders.
click here to find a list of TATM suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A TATM CEP of the European Pharmacopoeia monograph is often referred to as a TATM Certificate of Suitability (COS). The purpose of a TATM CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of TATM EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of TATM to their clients by showing that a TATM CEP has been issued for it. The manufacturer submits a TATM CEP (COS) as part of the market authorization procedure, and it takes on the role of a TATM CEP holder for the record. Additionally, the data presented in the TATM CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the TATM DMF.
A TATM CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. TATM 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 TATM suppliers with CEP (COS) on PharmaCompass.
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