01 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Oxethazaine "production-only"
01 1Taiwan
Oxethazaine "For Manufacturing Only"
Registration Number : 223MF10076
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2011-06-07
Latest Date of Registration : 2017-09-28
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PharmaCompass offers a list of Oxethazaine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Oxethazaine manufacturer or Oxethazaine supplier for your needs.
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A Emoren manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emoren, including repackagers and relabelers. The FDA regulates Emoren manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emoren API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Emoren manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Emoren supplier is an individual or a company that provides Emoren active pharmaceutical ingredient (API) or Emoren finished formulations upon request. The Emoren suppliers may include Emoren API manufacturers, exporters, distributors and traders.
click here to find a list of Emoren suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Emoren Drug Master File in Japan (Emoren JDMF) empowers Emoren API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Emoren JDMF during the approval evaluation for pharmaceutical products. At the time of Emoren JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Emoren suppliers with JDMF on PharmaCompass.
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