Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Cohance Lifesciences Limited
02 1FDC Limited
03 5Hy-Gro Chemicals Pharmtek Private Limited
04 1Vasudha Pharma Chem Limited
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2022-05-04
Registration Number : 20220504-209-J-1284
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : API Unit-I, RS 50/1,Mukteswarapuram Village, Jaggaiahpet Mandal, NTR District – 521...
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PharmaCompass offers a list of Flurbiprofen 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 Flurbiprofen manufacturer or Flurbiprofen supplier for your needs.
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A Acustop Cataplasma manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acustop Cataplasma, including repackagers and relabelers. The FDA regulates Acustop Cataplasma manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acustop Cataplasma 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 Acustop Cataplasma supplier is an individual or a company that provides Acustop Cataplasma active pharmaceutical ingredient (API) or Acustop Cataplasma finished formulations upon request. The Acustop Cataplasma suppliers may include Acustop Cataplasma API manufacturers, exporters, distributors and traders.
click here to find a list of Acustop Cataplasma 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 Acustop Cataplasma Drug Master File in Korea (Acustop Cataplasma KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Acustop Cataplasma. The MFDS reviews the Acustop Cataplasma KDMF as part of the drug registration process and uses the information provided in the Acustop Cataplasma KDMF to evaluate the safety and efficacy of the drug.
After submitting a Acustop Cataplasma 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 Acustop Cataplasma API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Acustop Cataplasma suppliers with KDMF on PharmaCompass.
We have 4 companies offering Acustop Cataplasma
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