Zach System is committed to providing Highly Customized Solutions for all your Development Programs.
01 2ZACH SYSTEM
02 1Moehs Cantabra, SL
03 1Kaikai Yuansheng Medicine Co., Ltd.
04 1Kaikai Yuansheng Medicine co., ltd
05 1Korea Biochem Pharmaceutical Co., Ltd.
06 1Korea Biochem Pharmaceutical Co., Ltd. @ Zhejiang East-Asia Pharmaceutical Co., Ltd.
07 1Korea United Biochem Pharmaceutical Co., Ltd.
08 1MFC Co., Ltd.@[Product Manufacturer Name] Suqian Ruixing Chemical Co.,Ltd._x000D_
09 1MFC Corporation
10 1Redox Bio Co., Ltd.
11 1Samjin Pharmaceutical Co., Ltd. @ [Manufacturer of Starting Material (Trimebutine)] Liaoning Benyuan Pharmaceutical Co., Ltd.
12 2Shanxi Shuangyan Pharmaceutical Co., Ltd.
13 13Xinhe Yuansheng Medicine Co., Ltd.
14 1Zhejiang East-Asia Pharmaceutical Chemical Co., Ltd
15 2Zhejiang East-Asia Pharmaceutical Co., Ltd
16 1Zhejiang East-Asia Pharmaceutical Co., Ltd,
17 22Zhejiang East-Asia Pharmaceutical Co., Ltd.
18 2Zhejiang East-Asia Pharmaceutical Co., Ltd. Ltd.
19 2Zhejiang East-Asia Pharmaceutical Co., Ltd._x000D_
20 1Zhejiang East-Asia Pharmaceutical Co.,Ltd
21 6Zhejiang East-Asia Pharmaceutical Co.,Ltd.
22 1Zhejiang East-asia Pharmaceutical Co., Ltd. Ltd.
23 1Zhejjang East-Asia Pharmaceutical Co., Ltd
Zach System is committed to providing Highly Customized Solutions for all your Development Programs.
Registrant Name : Samil Pharmaceutical Co., Ltd.
Registration Date : 2011-03-31
Registration Number : 20110331-13-B-310-07
Manufacturer Name : ZACH SYSTEM
Manufacturer Address : ZI La Corix Cadeau, 49240 Avrille, France
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2022-08-03
Registration Number : 20220803-13-B-463-14
Manufacturer Name : Moehs Cantabra, SL
Manufacturer Address : Poligono Industrial Requejada, Polanco 39313, Cantabria, Spain
Zach System is committed to providing Highly Customized Solutions for all your Development Programs.
Registrant Name : Samil Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-13-B-55-02
Manufacturer Name : ZACH SYSTEM
Manufacturer Address : ZI La Corix Cadeau, 49240 Avrille, France
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PharmaCompass offers a list of Trimebutine Maleate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Trimebutine Maleate manufacturer or Trimebutine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trimebutine Maleate manufacturer or Trimebutine Maleate supplier.
A Debridat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Debridat, including repackagers and relabelers. The FDA regulates Debridat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Debridat 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 Debridat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Debridat supplier is an individual or a company that provides Debridat active pharmaceutical ingredient (API) or Debridat finished formulations upon request. The Debridat suppliers may include Debridat API manufacturers, exporters, distributors and traders.
click here to find a list of Debridat suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Debridat Drug Master File in Korea (Debridat KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Debridat. The MFDS reviews the Debridat KDMF as part of the drug registration process and uses the information provided in the Debridat KDMF to evaluate the safety and efficacy of the drug.
After submitting a Debridat 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 Debridat API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Debridat suppliers with KDMF on PharmaCompass.
We have 9 companies offering Debridat
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