01 1BASF SE Ludwigshafen DE
02 1DSM Nutritional Products Ltd. Kaiseraugst CH
03 2DSM-FIRMENICH SWITZERLAND AG Kaiseraugst CH
01 1RRR-alpha-Tocopheryl acetate
02 2all-rac-alpha-Tocopheryl acetate
03 1alpha-Tocopheryl acetate concentrate (powder form), 50 g per 100 g of concentrate
01 1Germany
02 2Netherlands
03 1U.S.A
01 3Valid
02 1Withdrawn by Holder
All-rac-alpha-Tocopheryl Acetate
Certificate Number : R1-CEP 2005-040 - Rev 02
Status : Valid
Issue Date : 2023-06-29
Type : Chemical
Substance Number : 439
Alpha-Tocopheryl Acetate Concentrate (powder For...
Certificate Number : CEP 2019-086 - Rev 02
Status : Valid
Issue Date : 2025-12-19
Type : Chemical
Substance Number : 691
All-rac-alpha-Tocopheryl Acetate
Certificate Number : CEP 2001-180 - Rev 02
Status : Valid
Issue Date : 2025-07-18
Type : Chemical
Substance Number : 439
Certificate Number : R1-CEP 2001-320 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2014-10-17
Type : Chemical
Substance Number : 1257
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A CCRIS 6054 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCRIS 6054, including repackagers and relabelers. The FDA regulates CCRIS 6054 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCRIS 6054 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 CCRIS 6054 supplier is an individual or a company that provides CCRIS 6054 active pharmaceutical ingredient (API) or CCRIS 6054 finished formulations upon request. The CCRIS 6054 suppliers may include CCRIS 6054 API manufacturers, exporters, distributors and traders.
click here to find a list of CCRIS 6054 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A CCRIS 6054 CEP of the European Pharmacopoeia monograph is often referred to as a CCRIS 6054 Certificate of Suitability (COS). The purpose of a CCRIS 6054 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CCRIS 6054 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CCRIS 6054 to their clients by showing that a CCRIS 6054 CEP has been issued for it. The manufacturer submits a CCRIS 6054 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CCRIS 6054 CEP holder for the record. Additionally, the data presented in the CCRIS 6054 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CCRIS 6054 DMF.
A CCRIS 6054 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CCRIS 6054 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 CCRIS 6054 suppliers with CEP (COS) on PharmaCompass.
