Veranova: A CDMO that manages complexity with confidence.
01 3Macfarlan Smith Limited
02 1Toprak Mahsulleri Ofisi Genel Müdürlüğü
Veranova: A CDMO that manages complexity with confidence.
Registrant Name : Baeksu Pharmaceutical Co., Ltd.
Registration Date : 2021-07-13
Registration Number : 20190812-209-J-406(2)
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Veranova: A CDMO that manages complexity with confidence.
Registrant Name : Samung Industrial Co., Ltd.
Registration Date : 2019-08-12
Registration Number : 20190812-209-J-406
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, Scotland, United Kingdom
Veranova: A CDMO that manages complexity with confidence.
Registrant Name : Nosa Chemical Co., Ltd.
Registration Date : 2020-05-20
Registration Number : 20190812-209-J-406(1)
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, Scotland, United Kingdom
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PharmaCompass offers a list of Morphine Sulfate 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 Morphine Sulfate manufacturer or Morphine Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Morphine Sulfate manufacturer or Morphine Sulfate supplier.
PharmaCompass also assists you with knowing the Morphine Sulfate API Price utilized in the formulation of products. Morphine Sulfate API Price is not always fixed or binding as the Morphine Sulfate Price is obtained through a variety of data sources. The Morphine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Duromorph manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duromorph, including repackagers and relabelers. The FDA regulates Duromorph manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duromorph 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 Duromorph manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duromorph supplier is an individual or a company that provides Duromorph active pharmaceutical ingredient (API) or Duromorph finished formulations upon request. The Duromorph suppliers may include Duromorph API manufacturers, exporters, distributors and traders.
click here to find a list of Duromorph 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 Duromorph Drug Master File in Korea (Duromorph KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Duromorph. The MFDS reviews the Duromorph KDMF as part of the drug registration process and uses the information provided in the Duromorph KDMF to evaluate the safety and efficacy of the drug.
After submitting a Duromorph 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 Duromorph API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Duromorph suppliers with KDMF on PharmaCompass.
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