Veranova: A CDMO that manages complexity with confidence.
01 2Macfarlan Smith Limited
02 1Saneca Pharmaceuticals as
03 1Yichang Humanwell Pharmaceutical Co., Ltd.
Veranova: A CDMO that manages complexity with confidence.
Registrant Name : Baeksu Pharmaceutical Co., Ltd.
Registration Date : 2021-06-22
Registration Number : 20210622-210-J-918
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 : 2021-06-22
Registration Number : 20210622-210-J-918(A)
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
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PharmaCompass offers a list of Fentanyl Citrate 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 Fentanyl Citrate manufacturer or Fentanyl Citrate supplier for your needs.
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A LAZANDA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LAZANDA, including repackagers and relabelers. The FDA regulates LAZANDA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LAZANDA 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 LAZANDA supplier is an individual or a company that provides LAZANDA active pharmaceutical ingredient (API) or LAZANDA finished formulations upon request. The LAZANDA suppliers may include LAZANDA 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 LAZANDA Drug Master File in Korea (LAZANDA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of LAZANDA. The MFDS reviews the LAZANDA KDMF as part of the drug registration process and uses the information provided in the LAZANDA KDMF to evaluate the safety and efficacy of the drug.
After submitting a LAZANDA 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 LAZANDA API can apply through the Korea Drug Master File (KDMF).
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