Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
01 1PCAS Finland Oy
01 1Samoh Pharmaceutical Co., Ltd.
01 1Tetrahydrozoline hydrochloride
01 1France
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Tetrahydrozoline hydrochloride
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2024-03-11
Registration Number : 20240311-211-J-1616
Manufacturer Name : PCAS Finland Oy
Manufacturer Address : Messukentankatu 8, 20210 Turku, Finland
99
PharmaCompass offers a list of Tetrahydrozoline 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 Tetrahydrozoline manufacturer or Tetrahydrozoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetrahydrozoline manufacturer or Tetrahydrozoline supplier.
PharmaCompass also assists you with knowing the Tetrahydrozoline API Price utilized in the formulation of products. Tetrahydrozoline API Price is not always fixed or binding as the Tetrahydrozoline Price is obtained through a variety of data sources. The Tetrahydrozoline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Berberil N manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Berberil N, including repackagers and relabelers. The FDA regulates Berberil N manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Berberil N 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 Berberil N supplier is an individual or a company that provides Berberil N active pharmaceutical ingredient (API) or Berberil N finished formulations upon request. The Berberil N suppliers may include Berberil N 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 Berberil N Drug Master File in Korea (Berberil N KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Berberil N. The MFDS reviews the Berberil N KDMF as part of the drug registration process and uses the information provided in the Berberil N KDMF to evaluate the safety and efficacy of the drug.
After submitting a Berberil N 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 Berberil N API can apply through the Korea Drug Master File (KDMF).
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