Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 2Egis Pharmaceuticals PLC (Egis Pharmaceuticals Private Limited Company)
02 1Hanseochem Co., Ltd.
03 1Samhwa Biopharm Co., Ltd.
04 1Sanyo Chemical Laboratories Co., Ltd. Toyama Factory
05 1Symed Labs Ltd(Unit-I)
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Registrant Name : Hwanin Pharmaceutical Co., Ltd.
Registration Date : 2011-10-14
Registration Number : 20050831-64-C-192-03(1)
Manufacturer Name : Egis Pharmaceuticals PLC (Eg...
Manufacturer Address : H-1106 Budapest Kereszturi ut 30-38, Hungary
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-64-C-192-03
Manufacturer Name : Egis Pharmaceuticals PLC (Eg...
Manufacturer Address : H-1106 Budapest Kereszturi ut 30-38, Hungary
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PharmaCompass offers a list of Tofisopam 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 Tofisopam manufacturer or Tofisopam supplier for your needs.
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A DSSTox_CID_3681 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3681, including repackagers and relabelers. The FDA regulates DSSTox_CID_3681 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3681 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 DSSTox_CID_3681 supplier is an individual or a company that provides DSSTox_CID_3681 active pharmaceutical ingredient (API) or DSSTox_CID_3681 finished formulations upon request. The DSSTox_CID_3681 suppliers may include DSSTox_CID_3681 API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a DSSTox_CID_3681 Drug Master File in Korea (DSSTox_CID_3681 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DSSTox_CID_3681. The MFDS reviews the DSSTox_CID_3681 KDMF as part of the drug registration process and uses the information provided in the DSSTox_CID_3681 KDMF to evaluate the safety and efficacy of the drug.
After submitting a DSSTox_CID_3681 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 DSSTox_CID_3681 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of DSSTox_CID_3681 suppliers with KDMF on PharmaCompass.
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