01 3CDYMAX (INDIA) PHARMA PRIVATE LIMITED Bangalore IN
02 1CIPLA LIMITED Mumbai IN
03 1DEVA HOLDING A.Ş. Istanbul TR
04 1F.I.S. - Fabbrica Italiana Sintetici S.p.A. Montecchio Maggiore IT
05 3HETERO LABS LIMITED Hyderabad IN
06 1INTAS PHARMACEUTICALS LIMITED Ahmedabad IN
07 2LAURUS LABS LIMITED Hyderabad IN
08 1MSN LABORATORIES PRIVATE LIMITED Kardanur Village IN
09 1NATCO PHARMA LIMITED Hyderabad IN
10 1SHANDONG ANXIN PHARMACEUTICAL CO., LTD Jinan CN
11 1SHANDONG ANXIN PHARMACEUTICAL CO., LTD. Dongjia Town CN
12 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
13 1SIGNA S.A. DE C.V. Toluca MX
14 1SYNTHIMED LABS PRIVATE LIMITED Derabassi IN
15 1TAPI NL B.V. Amsterdam NL
16 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
17 1Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN
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PharmaCompass offers a list of Imatinib Mesylate 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 Imatinib Mesylate manufacturer or Imatinib Mesylate supplier for your needs.
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A UNII-8A1O1M485B manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-8A1O1M485B, including repackagers and relabelers. The FDA regulates UNII-8A1O1M485B manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-8A1O1M485B 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 UNII-8A1O1M485B supplier is an individual or a company that provides UNII-8A1O1M485B active pharmaceutical ingredient (API) or UNII-8A1O1M485B finished formulations upon request. The UNII-8A1O1M485B suppliers may include UNII-8A1O1M485B API manufacturers, exporters, distributors and traders.
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A UNII-8A1O1M485B CEP of the European Pharmacopoeia monograph is often referred to as a UNII-8A1O1M485B Certificate of Suitability (COS). The purpose of a UNII-8A1O1M485B CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of UNII-8A1O1M485B EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of UNII-8A1O1M485B to their clients by showing that a UNII-8A1O1M485B CEP has been issued for it. The manufacturer submits a UNII-8A1O1M485B CEP (COS) as part of the market authorization procedure, and it takes on the role of a UNII-8A1O1M485B CEP holder for the record. Additionally, the data presented in the UNII-8A1O1M485B CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the UNII-8A1O1M485B DMF.
A UNII-8A1O1M485B CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. UNII-8A1O1M485B 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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We have 15 companies offering UNII-8A1O1M485B
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