Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International Inc.
02 1AGC Inc.
03 1YS Life Science Co. , Ltd.
01 2Tafluprost
02 1Tafluprost
01 1Japan
02 1South Korea
03 1Taiwan
Chirogate is a professional Prostaglandin manufacturer.
Registration Number : 303MF10019
Registrant's Address : No. 2, Shih 4th Rd. , Yangmei Dist. , Taoyuan City 326013, Taiwan
Initial Date of Registration : 2021-01-26
Latest Date of Registration : 2022-11-09
Tafluprost "For manufacturing purposes only"
Registration Number : 304MF10024
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2022-02-02
Latest Date of Registration : 2022-02-02
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PharmaCompass offers a list of Tafluprost 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 Tafluprost manufacturer or Tafluprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tafluprost manufacturer or Tafluprost supplier.
PharmaCompass also assists you with knowing the Tafluprost API Price utilized in the formulation of products. Tafluprost API Price is not always fixed or binding as the Tafluprost Price is obtained through a variety of data sources. The Tafluprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zioptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zioptan, including repackagers and relabelers. The FDA regulates Zioptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zioptan 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 Zioptan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zioptan supplier is an individual or a company that provides Zioptan active pharmaceutical ingredient (API) or Zioptan finished formulations upon request. The Zioptan suppliers may include Zioptan API manufacturers, exporters, distributors and traders.
click here to find a list of Zioptan 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 Zioptan Drug Master File in Japan (Zioptan JDMF) empowers Zioptan 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 Zioptan JDMF during the approval evaluation for pharmaceutical products. At the time of Zioptan 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 Zioptan suppliers with JDMF on PharmaCompass.
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