Bal Pharma, leading manufacturer of niche & specialty API, Intermediates and Finished Formulations.
01 1BAL PHARMA LTD.
02 1Bal Pharma Limited.
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Bal Pharma, leading manufacturer of niche & specialty API, Intermediates and Finished Formulations.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2022-04-11
Registration Number : 20050831-1-C-2-02(1)
Manufacturer Name : Bal Pharma Limited.
Manufacturer Address : Plot No. 61B, Bommasandra Industrial Area, Hosur Road, Bangalore 560 099, India
Bal Pharma, leading manufacturer of niche & specialty API, Intermediates and Finished Formulations.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-1-C-2-02
Manufacturer Name : BAL PHARMA LTD.
Manufacturer Address : Plot No. 61B, Bommasandra Industrial area, Hosur Road, Bangalore - 560 099, India
A Gliclazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gliclazide, including repackagers and relabelers. The FDA regulates Gliclazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gliclazide 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 Gliclazide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gliclazide supplier is an individual or a company that provides Gliclazide active pharmaceutical ingredient (API) or Gliclazide finished formulations upon request. The Gliclazide suppliers may include Gliclazide API manufacturers, exporters, distributors and traders.
click here to find a list of Gliclazide 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 Gliclazide Drug Master File in Korea (Gliclazide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Gliclazide. The MFDS reviews the Gliclazide KDMF as part of the drug registration process and uses the information provided in the Gliclazide KDMF to evaluate the safety and efficacy of the drug.
After submitting a Gliclazide 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 Gliclazide API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Gliclazide suppliers with KDMF on PharmaCompass.
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