Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma s. r. o.
02 2Chirogate International Inc.
03 1EUROAPI Hungary Ltd.
04 2Cayman Chemical Company Incorporated.
05 1Kyowa Pharma Chemical Co., Ltd.
06 1Newchem S. p. A.
07 1Shanghai Tianwei Biopharmaceutical Co., Ltd.
08 1YS Life Science Co. , Ltd.
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
Registration Number : 302MF10040
Registrant's Address : ul. Pra(´)ce, 657, 277 11 Neratovice, Czech Republic
Initial Date of Registration : 2020-04-02
Latest Date of Registration : 2020-04-02
Chirogate is a professional Prostaglandin manufacturer.
Registration Number : 229MF10209
Registrant's Address : No. 2, Shih 4th Rd. , Yangmei Dist. , Taoyuan City 326013, Taiwan
Initial Date of Registration : 2017-12-01
Latest Date of Registration : 2022-09-08
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 225MF10111
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2013-05-30
Latest Date of Registration : 2024-12-18
Registration Number : 221MF10182
Registrant's Address : 1180 E. Ellsworth Road, Ann Arbor, MI 48108, USA
Initial Date of Registration : 2009-08-13
Latest Date of Registration : 2009-08-13
Chirogate is a professional Prostaglandin manufacturer.
Registration Number : 221MF10013
Registrant's Address : No. 2, Shih 4th Rd. , Yangmei Dist. , Taoyuan City 32657, Taiwan
Initial Date of Registration : 2009-01-13
Latest Date of Registration : 2020-03-09
Registration Number : 220MF10211
Registrant's Address : 1180 E. Ellsworth Road, Ann Arbor, MI 48108, USA
Initial Date of Registration : 2008-10-10
Latest Date of Registration : 2008-10-10
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PharmaCompass offers a list of Latanoprost 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 Latanoprost manufacturer or Latanoprost supplier for your needs.
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PharmaCompass also assists you with knowing the Latanoprost API Price utilized in the formulation of products. Latanoprost API Price is not always fixed or binding as the Latanoprost Price is obtained through a variety of data sources. The Latanoprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iopize manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iopize, including repackagers and relabelers. The FDA regulates Iopize manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iopize 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 Iopize manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iopize supplier is an individual or a company that provides Iopize active pharmaceutical ingredient (API) or Iopize finished formulations upon request. The Iopize suppliers may include Iopize API manufacturers, exporters, distributors and traders.
click here to find a list of Iopize 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 Iopize Drug Master File in Japan (Iopize JDMF) empowers Iopize 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 Iopize JDMF during the approval evaluation for pharmaceutical products. At the time of Iopize 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 Iopize suppliers with JDMF on PharmaCompass.
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