01 DISHMAN NETHERLANDS B.V. Veenendaal NL (2)
02 DSM Nutritional Products Ltd. Kaiseraugst CH (6)
03 FERMENTA BIOTECH LIMITED Thane (W) IN (3)
04 POLYMED THERAPEUTICS, INC. Houston US (1)
05 Solvay Pharmaceuticals BV Weesp NL (1)
06 ZHEJIANG GARDEN BIOCHEMICAL HIGH-TECH CO., LTD. Nanma CN (1)
01 Cholecalciferol (8)
02 Cholecalciferol concentrate (oily form), 1 000 000 IU/g, with all-rac-α-tocopherol in Trigylcerides, medium-chain (1)
03 Cholecalciferol concentrate (oily form), 1 000 000 IU/g, with all-rac-α-tocopherol, in Triglycerides, medium-chain (1)
04 Cholecalciferol concentrate (oily form), 2 000 000 IU/g in arachis oil (1)
05 Cholecalciferol concentrate (powder form), 100 000 IU/g, with all-rac-α-tocopherol (2)
06 Cholecalciferol, Site Sisseln (1)
01 Belgium (1)
02 China (1)
03 Gabon (1)
04 India (3)
05 Netherlands (3)
06 U.S.A (5)
01 Valid (10)
02 Withdrawn by Holder (4)
59
PharmaCompass offers a list of Vitamin D3 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 D3 manufacturer or Vitamin D3 supplier for your needs.
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A MolPort-001-740-051 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-740-051, including repackagers and relabelers. The FDA regulates MolPort-001-740-051 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-740-051 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 MolPort-001-740-051 supplier is an individual or a company that provides MolPort-001-740-051 active pharmaceutical ingredient (API) or MolPort-001-740-051 finished formulations upon request. The MolPort-001-740-051 suppliers may include MolPort-001-740-051 API manufacturers, exporters, distributors and traders.
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A MolPort-001-740-051 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-740-051 Certificate of Suitability (COS). The purpose of a MolPort-001-740-051 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-740-051 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-740-051 to their clients by showing that a MolPort-001-740-051 CEP has been issued for it. The manufacturer submits a MolPort-001-740-051 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-740-051 CEP holder for the record. Additionally, the data presented in the MolPort-001-740-051 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-740-051 DMF.
A MolPort-001-740-051 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-740-051 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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