01 2Ajinomoto Co. Inc. Kawasaki Plant
02 3Divi's Laboratories Limited (Unit-2)
03 2Shandong Xinhua Pharmaceutical Co., Ltd
04 1Zhejiang Huahai Pharmaceutical Co., Ltd
05 1Zhejiang Wild Wind Pharmaceutical Co., Ltd
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PharmaCompass offers a list of Etilevodopa 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 Etilevodopa manufacturer or Etilevodopa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etilevodopa manufacturer or Etilevodopa supplier.
PharmaCompass also assists you with knowing the Etilevodopa API Price utilized in the formulation of products. Etilevodopa API Price is not always fixed or binding as the Etilevodopa Price is obtained through a variety of data sources. The Etilevodopa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Biodopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biodopa, including repackagers and relabelers. The FDA regulates Biodopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biodopa 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 Biodopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Biodopa supplier is an individual or a company that provides Biodopa active pharmaceutical ingredient (API) or Biodopa finished formulations upon request. The Biodopa suppliers may include Biodopa API manufacturers, exporters, distributors and traders.
click here to find a list of Biodopa 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 Biodopa Drug Master File in Korea (Biodopa KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Biodopa. The MFDS reviews the Biodopa KDMF as part of the drug registration process and uses the information provided in the Biodopa KDMF to evaluate the safety and efficacy of the drug.
After submitting a Biodopa 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 Biodopa API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Biodopa suppliers with KDMF on PharmaCompass.
We have 5 companies offering Biodopa
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