Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak as
02 1Carbogen AMCIS AG
03 1Centaur Pharmaceuticals Private Limited
04 1INDOCO REMEDIES LIMITED
05 1Laurus Labs Limited
06 2MEDICHEM SA
07 1Piramal Pharma Limited
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registrant Name : Hiple Co., Ltd.
Registration Date : 2013-12-20
Registration Number : 20131220-200-I-380-02
Manufacturer Name : Farmak as
Manufacturer Address : Na Vlcinci 16/3, Klasterni Hradisko, 779 00 Olomouc, Czech Republic
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PharmaCompass offers a list of Brimonidine Tartrate 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 Brimonidine Tartrate manufacturer or Brimonidine Tartrate supplier for your needs.
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A 59803-98-4 (Parent) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 59803-98-4 (Parent), including repackagers and relabelers. The FDA regulates 59803-98-4 (Parent) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 59803-98-4 (Parent) 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 59803-98-4 (Parent) supplier is an individual or a company that provides 59803-98-4 (Parent) active pharmaceutical ingredient (API) or 59803-98-4 (Parent) finished formulations upon request. The 59803-98-4 (Parent) suppliers may include 59803-98-4 (Parent) API manufacturers, exporters, distributors and traders.
click here to find a list of 59803-98-4 (Parent) 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 59803-98-4 (Parent) Drug Master File in Korea (59803-98-4 (Parent) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 59803-98-4 (Parent). The MFDS reviews the 59803-98-4 (Parent) KDMF as part of the drug registration process and uses the information provided in the 59803-98-4 (Parent) KDMF to evaluate the safety and efficacy of the drug.
After submitting a 59803-98-4 (Parent) 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 59803-98-4 (Parent) API can apply through the Korea Drug Master File (KDMF).
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