01 1CHEMPORT INC. Naju-si KR
02 1SELJEL JELATIN SANAYI VE TICARET A.Ş Istanbul TR
01 1Fish oil, rich in omega-3-acids, Type I
02 1Gelatin, Caustic and lime hide gelatin
01 1South Korea
02 1Turkey
01 2Valid
Fish Oil, Rich In Omega-3-acids, Type I
Certificate Number : R1-CEP 2015-282 - Rev 00
Status : Valid
Issue Date : 2022-03-17
Type : Chemical
Substance Number : 1912
Gelatin, Caustic And Lime Hide Gelatin
Certificate Number : R0-CEP 2021-504 - Rev 00
Status : Valid
Issue Date : 2022-06-02
Type : TSE
Substance Number : 330
93
PharmaCompass offers a list of Tetrahydrocannabinol 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 Tetrahydrocannabinol manufacturer or Tetrahydrocannabinol supplier for your needs.
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A Marinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Marinol, including repackagers and relabelers. The FDA regulates Marinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Marinol 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 Marinol supplier is an individual or a company that provides Marinol active pharmaceutical ingredient (API) or Marinol finished formulations upon request. The Marinol suppliers may include Marinol API manufacturers, exporters, distributors and traders.
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A Marinol CEP of the European Pharmacopoeia monograph is often referred to as a Marinol Certificate of Suitability (COS). The purpose of a Marinol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Marinol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Marinol to their clients by showing that a Marinol CEP has been issued for it. The manufacturer submits a Marinol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Marinol CEP holder for the record. Additionally, the data presented in the Marinol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Marinol DMF.
A Marinol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Marinol 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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