01 1Dynamit Nobel GmbH
01 1Encomac Co., Ltd.
01 1nitroglycerin
01 1Germany
Registrant Name : Encomac Co., Ltd.
Registration Date : 2021-11-10
Registration Number : 20211110-210-J-1146
Manufacturer Name : Dynamit Nobel GmbH
Manufacturer Address : D-51377, Kalkstrasse 218 Leverkusen, Germany
38
PharmaCompass offers a list of Nitroglycerin 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 Nitroglycerin manufacturer or Nitroglycerin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nitroglycerin manufacturer or Nitroglycerin supplier.
A NitroQuick manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NitroQuick, including repackagers and relabelers. The FDA regulates NitroQuick manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NitroQuick 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 NitroQuick manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A NitroQuick supplier is an individual or a company that provides NitroQuick active pharmaceutical ingredient (API) or NitroQuick finished formulations upon request. The NitroQuick suppliers may include NitroQuick API manufacturers, exporters, distributors and traders.
click here to find a list of NitroQuick 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 NitroQuick Drug Master File in Korea (NitroQuick KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of NitroQuick. The MFDS reviews the NitroQuick KDMF as part of the drug registration process and uses the information provided in the NitroQuick KDMF to evaluate the safety and efficacy of the drug.
After submitting a NitroQuick 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 NitroQuick API can apply through the Korea Drug Master File (KDMF).
click here to find a list of NitroQuick suppliers with KDMF on PharmaCompass.
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