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01 Dongguk Life Science Co., Ltd. (2)
02 ENGCHEM Life Science Co., Ltd. (1)
03 STech Pharma Co., Ltd. (1)
01 Dongguk Life Science Co., Ltd. (2)
02 ENGCHEM Life Science Co., Ltd. (1)
03 STech Pharma Co., Ltd. (1)
01 dota (4)
01 South Korea (3)
02 Blank (1)
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PharmaCompass offers a list of DOTA 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 DOTA manufacturer or DOTA supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred DOTA manufacturer or DOTA supplier.
PharmaCompass also assists you with knowing the DOTA API Price utilized in the formulation of products. DOTA API Price is not always fixed or binding as the DOTA Price is obtained through a variety of data sources. The DOTA Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DOTA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DOTA, including repackagers and relabelers. The FDA regulates DOTA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DOTA 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 DOTA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DOTA supplier is an individual or a company that provides DOTA active pharmaceutical ingredient (API) or DOTA finished formulations upon request. The DOTA suppliers may include DOTA API manufacturers, exporters, distributors and traders.
click here to find a list of DOTA 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 DOTA Drug Master File in Korea (DOTA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DOTA. The MFDS reviews the DOTA KDMF as part of the drug registration process and uses the information provided in the DOTA KDMF to evaluate the safety and efficacy of the drug.
After submitting a DOTA 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 DOTA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of DOTA suppliers with KDMF on PharmaCompass.
We have 2 companies offering DOTA
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