01 1Procos SPA
01 1Sungjin Exim Co., Ltd.
01 1Pyridostigmine Bromide
01 1Italy
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2021-05-12
Registration Number : 20210512-211-J-632
Manufacturer Name : Procos SPA
Manufacturer Address : Viamatteotti 249, Cameri(Novara)28062 Italy
89
PharmaCompass offers a list of Pyridostigmine 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 Pyridostigmine manufacturer or Pyridostigmine supplier for your needs.
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PharmaCompass also assists you with knowing the Pyridostigmine API Price utilized in the formulation of products. Pyridostigmine API Price is not always fixed or binding as the Pyridostigmine Price is obtained through a variety of data sources. The Pyridostigmine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lefaxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lefaxin, including repackagers and relabelers. The FDA regulates Lefaxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lefaxin 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 Lefaxin supplier is an individual or a company that provides Lefaxin active pharmaceutical ingredient (API) or Lefaxin finished formulations upon request. The Lefaxin suppliers may include Lefaxin 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 Lefaxin Drug Master File in Korea (Lefaxin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lefaxin. The MFDS reviews the Lefaxin KDMF as part of the drug registration process and uses the information provided in the Lefaxin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lefaxin 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 Lefaxin API can apply through the Korea Drug Master File (KDMF).
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