01 BASF SE Ludwigshafen DE (1)
02 DSM Nutritional Products Ltd. Kaiseraugst CH (2)
01 Vitamin A concentrate (powder form), synthetic, Palmitate, 250000 IU/g, with all-rac-alpha-tocopherol (1)
02 Vitamin A, 2.8 MIU/g, acetate (1)
03 Vitamin A, Not less than 1.7 MIU/g, palmitate (1)
01 Germany (1)
02 Netherlands (2)
01 Valid (3)
52
PharmaCompass offers a list of Vitamin A 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 A manufacturer or Vitamin A supplier for your needs.
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PharmaCompass also assists you with knowing the Vitamin A API Price utilized in the formulation of products. Vitamin A API Price is not always fixed or binding as the Vitamin A Price is obtained through a variety of data sources. The Vitamin A Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300287 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300287, including repackagers and relabelers. The FDA regulates Tox21_300287 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300287 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 Tox21_300287 supplier is an individual or a company that provides Tox21_300287 active pharmaceutical ingredient (API) or Tox21_300287 finished formulations upon request. The Tox21_300287 suppliers may include Tox21_300287 API manufacturers, exporters, distributors and traders.
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A Tox21_300287 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300287 Certificate of Suitability (COS). The purpose of a Tox21_300287 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300287 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300287 to their clients by showing that a Tox21_300287 CEP has been issued for it. The manufacturer submits a Tox21_300287 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300287 CEP holder for the record. Additionally, the data presented in the Tox21_300287 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300287 DMF.
A Tox21_300287 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300287 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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