01 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Japan Bureau Clofibrate (for manufacturing only)
01 1Taiwan
Japanese Pharmacopoeia Clofibrate (for manufacturing purposes only)
Registration Number : 218MF10071
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2010-04-05
81
PharmaCompass offers a list of Clofibrate 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 Clofibrate manufacturer or Clofibrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clofibrate manufacturer or Clofibrate supplier.
A Clofar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clofar, including repackagers and relabelers. The FDA regulates Clofar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clofar API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Clofar supplier is an individual or a company that provides Clofar active pharmaceutical ingredient (API) or Clofar finished formulations upon request. The Clofar suppliers may include Clofar API manufacturers, exporters, distributors and traders.
click here to find a list of Clofar 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 Clofar Drug Master File in Japan (Clofar JDMF) empowers Clofar 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 Clofar JDMF during the approval evaluation for pharmaceutical products. At the time of Clofar 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 Clofar suppliers with JDMF on PharmaCompass.
We have 1 companies offering Clofar
Get in contact with the supplier of your choice:
