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