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 INNOVAR-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INNOVAR-1, including repackagers and relabelers. The FDA regulates INNOVAR-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INNOVAR-1 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 INNOVAR-1 supplier is an individual or a company that provides INNOVAR-1 active pharmaceutical ingredient (API) or INNOVAR-1 finished formulations upon request. The INNOVAR-1 suppliers may include INNOVAR-1 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 INNOVAR-1 Drug Master File in Korea (INNOVAR-1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of INNOVAR-1. The MFDS reviews the INNOVAR-1 KDMF as part of the drug registration process and uses the information provided in the INNOVAR-1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a INNOVAR-1 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 INNOVAR-1 API can apply through the Korea Drug Master File (KDMF).
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