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
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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 DSSTox_RID_77069 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_RID_77069, including repackagers and relabelers. The FDA regulates DSSTox_RID_77069 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_RID_77069 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 DSSTox_RID_77069 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DSSTox_RID_77069 supplier is an individual or a company that provides DSSTox_RID_77069 active pharmaceutical ingredient (API) or DSSTox_RID_77069 finished formulations upon request. The DSSTox_RID_77069 suppliers may include DSSTox_RID_77069 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_RID_77069 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 DSSTox_RID_77069 Drug Master File in Korea (DSSTox_RID_77069 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DSSTox_RID_77069. The MFDS reviews the DSSTox_RID_77069 KDMF as part of the drug registration process and uses the information provided in the DSSTox_RID_77069 KDMF to evaluate the safety and efficacy of the drug.
After submitting a DSSTox_RID_77069 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 DSSTox_RID_77069 API can apply through the Korea Drug Master File (KDMF).
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