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