Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma s. r. o.
02 1EUROAPI Hungary Ltd.
03 1YS Life Science Co. , Ltd.
01 2Travoprost
02 1Travoprost "production-only"
01 1Czech Republic
02 1France
03 1South Korea
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
Registration Number : 227MF10153
Registrant's Address : ul. Pra(´)ce 657,277 11 Neratovice, Czech Republic
Initial Date of Registration : 2015-06-01
Latest Date of Registration : 2022-09-14
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 227MF10136
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2015-05-12
Latest Date of Registration : 2017-01-13
Travoprost "For manufacturing only"
Registration Number : 227MF10195
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2015-08-03
Latest Date of Registration : 2015-08-03
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PharmaCompass offers a list of Travoprost 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 Travoprost manufacturer or Travoprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Travoprost manufacturer or Travoprost supplier.
PharmaCompass also assists you with knowing the Travoprost API Price utilized in the formulation of products. Travoprost API Price is not always fixed or binding as the Travoprost Price is obtained through a variety of data sources. The Travoprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IZBA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IZBA, including repackagers and relabelers. The FDA regulates IZBA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IZBA 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 IZBA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A IZBA supplier is an individual or a company that provides IZBA active pharmaceutical ingredient (API) or IZBA finished formulations upon request. The IZBA suppliers may include IZBA API manufacturers, exporters, distributors and traders.
click here to find a list of IZBA 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 IZBA Drug Master File in Japan (IZBA JDMF) empowers IZBA 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 IZBA JDMF during the approval evaluation for pharmaceutical products. At the time of IZBA 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 IZBA suppliers with JDMF on PharmaCompass.
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