01 1M/s BDR Lifesciences Pvt Ltd
02 1M/s BDR lifesciences Pvt Ltd
03 1M/s Cdymax India Pharma Pvt Ltd
04 1M/s Cipla Limited
05 1M/s Gland Chemicals Pvt Ltd
06 2M/s Hetero Labs Ltd
07 1M/s Laurus Labs Limited
08 1M/s Laurus labs Limited
09 2M/s Natco Pharma Limited
10 1M/s Reliance Life Sciences Pvt ltd
11 1M/s Sakar Healthcare limited
12 1M/s Shilpa Pharma Lifesciences Ltd
13 1M/s Suven Life Sciences Limited
14 1M/s Synthimed Labs Private Limited
15 1M/sFresenius Kabi Oncology Ltd
16 1M/sMSN laboratories Pvt Lt
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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 written confirmation (UNII-8A1O1M485B WC) is an official document issued by a regulatory agency to a UNII-8A1O1M485B manufacturer, verifying that the manufacturing facility of a UNII-8A1O1M485B active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting UNII-8A1O1M485B APIs or UNII-8A1O1M485B finished pharmaceutical products to another nation, regulatory agencies frequently require a UNII-8A1O1M485B WC (written confirmation) as part of the regulatory process.
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