01 1C.S. Bio Co.
02 1Peptisyntha, Inc.
01 1Nafarelin acetate
02 1Nafarelin acetate "Mitsuba"
01 1Germany
02 1U.S.A
Registration Number : 218MF10511
Registrant's Address : 20910 Higgins Court Torrance, California USA 90501-1722
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2006-05-18
Registration Number : 225MF10109
Registrant's Address : 20 Kelly Court, Menlo Park, CA 94025 USA
Initial Date of Registration : 2013-05-30
Latest Date of Registration : 2018-09-03
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PharmaCompass offers a list of Nafarelin Acetate 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 Nafarelin Acetate manufacturer or Nafarelin Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nafarelin Acetate manufacturer or Nafarelin Acetate supplier.
PharmaCompass also assists you with knowing the Nafarelin Acetate API Price utilized in the formulation of products. Nafarelin Acetate API Price is not always fixed or binding as the Nafarelin Acetate Price is obtained through a variety of data sources. The Nafarelin Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Synarel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Synarel, including repackagers and relabelers. The FDA regulates Synarel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Synarel 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 Synarel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Synarel supplier is an individual or a company that provides Synarel active pharmaceutical ingredient (API) or Synarel finished formulations upon request. The Synarel suppliers may include Synarel API manufacturers, exporters, distributors and traders.
click here to find a list of Synarel 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 Synarel Drug Master File in Japan (Synarel JDMF) empowers Synarel 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 Synarel JDMF during the approval evaluation for pharmaceutical products. At the time of Synarel 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 Synarel suppliers with JDMF on PharmaCompass.
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