01 CHEMCO PLUS SCIENTIFIC CO LTD (1)
02 DAISO CO LTD (2)
03 FUJI SILYSIA CHEMICAL LTD (3)
04 Fuji Chemical Industry (1)
05 Glassven (1)
06 Henan Minmetals East Industrial (1)
07 Hubei Huifu Nanomaterial (1)
08 JIAZHONG NOVEL MATERIAL CORP (3)
09 Mallinckrodt Pharmaceuticals (2)
10 PQ Corporation (1)
11 Pfizer Inc (1)
12 Sanmar Holdings Limited (3)
13 Wacker Chemie AG (1)
14 YMC Co. Ltd. (1)
15 YMC Europe GmbH (1)
16 Blank (2)
01 ABX AND CBX BONDED PHASE SILICA GELS (1)
02 AEROSIL (1)
03 BONDED SILICA MICROSPHERE (1)
04 CAB-O-SIL GRADE M-5 (FUMED SILICA) (1)
05 CAB-O-SIL M-5P FUMED SILICA (1)
06 CAB-O-SIL TS-610P HYDROPHOBIC COLLOIDAL FUMED SILICA (1)
07 COLLOIDAL SILICON DIOXIDE (1)
08 DAISOGEL ODS SERIES CHEMICALLY MODIFIED SILICA GEL (1)
09 DAISOGEL SP-C8 SERIES CHEMICALLY MODIFIED SILICA GEL (1)
10 FUJISIL (SILICON DIOXIDE USP/NF) (1)
11 HDK N20 PHARMA (1)
12 HYBRID SILICA MICROSPHERE (1)
13 LC-SORB SPW-C-ODS(S) (1)
14 LUDOX (1)
15 PEI BONDED PHASE SILICA GEL (1)
16 PRECIPITATED SILICA (1)
17 SILICA MICROSPHERE (1)
18 SILICON DIOXIDE (1)
19 SORBOSIL(R) AC43, SYNTHETIC AMORPHOUS SILICA PRECIPITATE (1)
20 SYNTHETIC AMORPHOUS SILICA FOR CHROMATOGRAPHY PRODUCTS - CHROMATOREX (1)
21 SYNTHETIC AMORPHOUS SILICA FOR NORMAL PHASE CHROMATOGRAPHY PRODUCTS - CHROMATOREX (1)
22 SYNTHETIC AMORPHOUS SILICA PRODUCTS - SYLYSIA/ADSOLIDER (1)
23 YMC * GEL (1)
24 YMC-TRIART (1)
25 ZORBAX (1)
01 China (6)
02 Germany (2)
03 India (3)
04 Ireland (2)
05 Japan (8)
06 U.S.A (2)
07 Blank (2)
01 Active (18)
02 Inactive (7)
01 Blank (25)
71
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A MolPort-001-756-349 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-756-349, including repackagers and relabelers. The FDA regulates MolPort-001-756-349 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-756-349 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-001-756-349 supplier is an individual or a company that provides MolPort-001-756-349 active pharmaceutical ingredient (API) or MolPort-001-756-349 finished formulations upon request. The MolPort-001-756-349 suppliers may include MolPort-001-756-349 API manufacturers, exporters, distributors and traders.
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A MolPort-001-756-349 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-756-349 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-756-349 DMFs exist exist since differing nations have different regulations, such as MolPort-001-756-349 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-756-349 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-756-349 USDMF includes data on MolPort-001-756-349's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-756-349 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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