Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 2Cohance Lifesciences Limited
02 1FDC Limited
03 5Hy-Gro Chemicals Pharmtek Private Limited
04 1Integrin Life Sciences Pvt. Ltd.
05 1Vasudha Pharma Chem Limited
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Medipoem Co., Ltd.
Registration Date : 2025-05-26
Registration Number : 20220504-209-J-1284(A)
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : API Unit-I, RS 50/1, Mukteswarapuram Village, Jaggaiahpet Mandal, NTR District – 52...
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flurbiprofen manufacturer or Flurbiprofen supplier.
PharmaCompass also assists you with knowing the Flurbiprofen API Price utilized in the formulation of products. Flurbiprofen API Price is not always fixed or binding as the Flurbiprofen Price is obtained through a variety of data sources. The Flurbiprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anside manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anside, including repackagers and relabelers. The FDA regulates Anside manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anside API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Anside manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Anside supplier is an individual or a company that provides Anside active pharmaceutical ingredient (API) or Anside finished formulations upon request. The Anside suppliers may include Anside API manufacturers, exporters, distributors and traders.
click here to find a list of Anside 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 Anside Drug Master File in Korea (Anside KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Anside. The MFDS reviews the Anside KDMF as part of the drug registration process and uses the information provided in the Anside KDMF to evaluate the safety and efficacy of the drug.
After submitting a Anside 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 Anside API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Anside suppliers with KDMF on PharmaCompass.
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