01 1NEWCHEM SpA@IMS . SrI@Zhejiang Xianju Pharmaceutical Co., Ltd
01 1Sungjin Exim Co., Ltd.
01 1Prednicarbate
01 1Italy
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2020-06-05
Registration Number : 20200605-211-J-650
Manufacturer Name : NEWCHEM SpA@IMS . SrI@Zhejia...
Manufacturer Address : Via Roveggia, 47-37136 Verona(VR) Italy@Via Venezia Giulia 23-20157 Milano(MI) Italy@...
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PharmaCompass offers a list of Prednicarbate 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 Prednicarbate manufacturer or Prednicarbate supplier for your needs.
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PharmaCompass also assists you with knowing the Prednicarbate API Price utilized in the formulation of products. Prednicarbate API Price is not always fixed or binding as the Prednicarbate Price is obtained through a variety of data sources. The Prednicarbate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Batmen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Batmen, including repackagers and relabelers. The FDA regulates Batmen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Batmen 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 Batmen supplier is an individual or a company that provides Batmen active pharmaceutical ingredient (API) or Batmen finished formulations upon request. The Batmen suppliers may include Batmen 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 Batmen Drug Master File in Korea (Batmen KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Batmen. The MFDS reviews the Batmen KDMF as part of the drug registration process and uses the information provided in the Batmen KDMF to evaluate the safety and efficacy of the drug.
After submitting a Batmen 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 Batmen API can apply through the Korea Drug Master File (KDMF).
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