Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
01 1BASF Pharma (Evionnaz) SA
02 3Siegfried PharmaChemikalien Minden GmbH
03 1CTX Life Sciences Pvt. Ltd
04 6CTX Life Sciences Pvt. Ltd.
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Registrant Name : Johnson & Johnson Korea Sales Co., Ltd.
Registration Date : 2024-07-17
Registration Number : 20130806-189-I-304-02(2)
Manufacturer Name : Siegfried PharmaChemikalien ...
Manufacturer Address : Karlstrasse 15-39, 42-44, 32423 Minden, North Rhine-Westphalia, Germany
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Registrant Name : CTC Bio Co., Ltd.
Registration Date : 2019-10-28
Registration Number : 20130806-189-I-304-02(1)
Manufacturer Name : Siegfried PharmaChemikalien ...
Manufacturer Address : Karlstrasse 15-39, 42-44, 32423 Minden, North Rhine-Westphalia, Germany
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Registrant Name : Heilion Korea Co., Ltd.
Registration Date : 2012-06-01
Registration Number : 20120601-189-I-31-01
Manufacturer Name : BASF Pharma (Evionnaz) SA
Manufacturer Address : Route du Simplon 1, 36, 1902 Evionnaz, Switzerland
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Registrant Name : Dongwha Pharmaceutical Co., Ltd.
Registration Date : 2013-08-06
Registration Number : 20130806-189-I-304-02
Manufacturer Name : Siegfried PharmaChemikalien ...
Manufacturer Address : Karlstraße 15-39, 42-44 32423 Minden, Germany
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PharmaCompass offers a list of Xylometazoline Hydrochloride 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 Xylometazoline Hydrochloride manufacturer or Xylometazoline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Xylometazoline Hydrochloride manufacturer or Xylometazoline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Xylometazoline Hydrochloride API Price utilized in the formulation of products. Xylometazoline Hydrochloride API Price is not always fixed or binding as the Xylometazoline Hydrochloride Price is obtained through a variety of data sources. The Xylometazoline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A schnupfen endrine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of schnupfen endrine, including repackagers and relabelers. The FDA regulates schnupfen endrine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. schnupfen endrine 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 schnupfen endrine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A schnupfen endrine supplier is an individual or a company that provides schnupfen endrine active pharmaceutical ingredient (API) or schnupfen endrine finished formulations upon request. The schnupfen endrine suppliers may include schnupfen endrine API manufacturers, exporters, distributors and traders.
click here to find a list of schnupfen endrine 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 schnupfen endrine Drug Master File in Korea (schnupfen endrine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of schnupfen endrine. The MFDS reviews the schnupfen endrine KDMF as part of the drug registration process and uses the information provided in the schnupfen endrine KDMF to evaluate the safety and efficacy of the drug.
After submitting a schnupfen endrine 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 schnupfen endrine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of schnupfen endrine suppliers with KDMF on PharmaCompass.
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