Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 2FARMAK, a. s.
02 1YS Life Science Co. , Ltd.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registration Number : 306MF10119
Registrant's Address : Na vlcinci 16/3 Klasterni Hradisko 77900 Olomouc Czech Republic
Initial Date of Registration : 2024-09-03
Latest Date of Registration : 2024-09-03
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registration Number : 230MF10078
Registrant's Address : Na vlcinci 16/3 Klasterni Hradisko 77900 Olomouc Czech Republic
Initial Date of Registration : 2018-07-03
Latest Date of Registration : 2018-07-03
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PharmaCompass offers a list of Bromfenac Sodium 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 Bromfenac Sodium manufacturer or Bromfenac Sodium supplier for your needs.
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A Bromfenac ophthalmic solution manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromfenac ophthalmic solution, including repackagers and relabelers. The FDA regulates Bromfenac ophthalmic solution manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromfenac ophthalmic solution API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Bromfenac ophthalmic solution supplier is an individual or a company that provides Bromfenac ophthalmic solution active pharmaceutical ingredient (API) or Bromfenac ophthalmic solution finished formulations upon request. The Bromfenac ophthalmic solution suppliers may include Bromfenac ophthalmic solution API manufacturers, exporters, distributors and traders.
click here to find a list of Bromfenac ophthalmic solution 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 Bromfenac ophthalmic solution Drug Master File in Japan (Bromfenac ophthalmic solution JDMF) empowers Bromfenac ophthalmic solution 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 Bromfenac ophthalmic solution JDMF during the approval evaluation for pharmaceutical products. At the time of Bromfenac ophthalmic solution 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 Bromfenac ophthalmic solution suppliers with JDMF on PharmaCompass.
We have 2 companies offering Bromfenac ophthalmic solution
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