01 1ARCHER DANIELS MIDLAND COMPANY Decatur US
02 1BASF SE Ludwigshafen DE
03 1Croda Europe Limited Leek GB
04 1DSM Nutritional Products Ltd. Kaiseraugst CH
01 1Omega-3-acid triglycerides, Grade SF 07100, with tocopherols
02 1RRR-alpha-Tocopherol
03 2all-rac-alpha-Tocopherol
01 1Germany
02 2U.S.A
03 1United Kingdom
01 4Valid
Certificate Number : R1-CEP 2016-184 - Rev 00
Status : Valid
Issue Date : 2023-02-14
Type : Chemical
Substance Number : 1256
Certificate Number : R1-CEP 2005-039 - Rev 02
Status : Valid
Issue Date : 2023-06-30
Type : Chemical
Substance Number : 692
Omega-3-acid Triglycerides, Grade SF 07100, With...
Certificate Number : R1-CEP 2001-419 - Rev 03
Status : Valid
Issue Date : 2016-08-12
Type : Chemical
Substance Number : 1352
Certificate Number : R0-CEP 2019-164 - Rev 00
Status : Valid
Issue Date : 2021-02-11
Type : Chemical
Substance Number : 692
88
PharmaCompass offers a list of Vitamin E 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 Vitamin E manufacturer or Vitamin E supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin E manufacturer or Vitamin E supplier.
PharmaCompass also assists you with knowing the Vitamin E API Price utilized in the formulation of products. Vitamin E API Price is not always fixed or binding as the Vitamin E Price is obtained through a variety of data sources. The Vitamin E Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A P500 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of P500, including repackagers and relabelers. The FDA regulates P500 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. P500 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 P500 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A P500 supplier is an individual or a company that provides P500 active pharmaceutical ingredient (API) or P500 finished formulations upon request. The P500 suppliers may include P500 API manufacturers, exporters, distributors and traders.
click here to find a list of P500 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A P500 CEP of the European Pharmacopoeia monograph is often referred to as a P500 Certificate of Suitability (COS). The purpose of a P500 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of P500 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of P500 to their clients by showing that a P500 CEP has been issued for it. The manufacturer submits a P500 CEP (COS) as part of the market authorization procedure, and it takes on the role of a P500 CEP holder for the record. Additionally, the data presented in the P500 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the P500 DMF.
A P500 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. P500 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 P500 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering P500
Get in contact with the supplier of your choice:
