01 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Japan Bureau Clofibrate (for manufacturing only)
01 1Taiwan
Japanese Pharmacopoeia Clofibrate (for manufacturing 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
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PharmaCompass offers a list of Clofibrate 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 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.
PharmaCompass also assists you with knowing the Clofibrate API Price utilized in the formulation of products. Clofibrate API Price is not always fixed or binding as the Clofibrate Price is obtained through a variety of data sources. The Clofibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ELPI manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ELPI, including repackagers and relabelers. The FDA regulates ELPI manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ELPI 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 ELPI supplier is an individual or a company that provides ELPI active pharmaceutical ingredient (API) or ELPI finished formulations upon request. The ELPI suppliers may include ELPI API manufacturers, exporters, distributors and traders.
click here to find a list of ELPI suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 ELPI Drug Master File in Japan (ELPI JDMF) empowers ELPI 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 ELPI JDMF during the approval evaluation for pharmaceutical products. At the time of ELPI 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 ELPI suppliers with JDMF on PharmaCompass.
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