DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories (EU) Ltd
02 1YS Life Science Co., Ltd.
01 1Novartis Korea Ltd.
02 1YS Life Science Co., Ltd.
01 2Travofrost
01 1India
02 1South Korea
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registrant Name : Novartis Korea Ltd.
Registration Date : 2012-11-08
Registration Number : 20121108-208-I-101-01
Manufacturer Name : Dr. Reddy's Laboratories (EU...
Manufacturer Address : Steanard Lane, Mirfield, West Yorkshire, WF14 8HZ
Registrant Name : YS Life Science Co., Ltd.
Registration Date : 2017-06-23
Registration Number : 20170623-208-I-528-02
Manufacturer Name : YS Life Science Co., Ltd.
Manufacturer Address : 207 Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do
63
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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a IZBA Drug Master File in Korea (IZBA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of IZBA. The MFDS reviews the IZBA KDMF as part of the drug registration process and uses the information provided in the IZBA KDMF to evaluate the safety and efficacy of the drug.
After submitting a IZBA KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their IZBA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of IZBA suppliers with KDMF on PharmaCompass.
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