01 1SM Biomed SDN.BHD.
01 1Hiple Co., Ltd.
01 1Erythromycin
01 1Malaysia
Registrant Name : Hiple Co., Ltd.
Registration Date : 2015-11-17
Registration Number : 20120601-107-F-64-02(1)
Manufacturer Name : SM Biomed SDN.BHD.
Manufacturer Address : Lot 90, Sungai Petani Industrial Estate, 08000 Sungai Petani, Kedah, Malaysia (Erythr...
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PharmaCompass offers a list of Erythromycin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Erythromycin manufacturer or Erythromycin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Erythromycin manufacturer or Erythromycin supplier.
A Pantoderm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pantoderm, including repackagers and relabelers. The FDA regulates Pantoderm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pantoderm 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 Pantoderm manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Pantoderm supplier is an individual or a company that provides Pantoderm active pharmaceutical ingredient (API) or Pantoderm finished formulations upon request. The Pantoderm suppliers may include Pantoderm API manufacturers, exporters, distributors and traders.
click here to find a list of Pantoderm suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Pantoderm Drug Master File in Korea (Pantoderm KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pantoderm. The MFDS reviews the Pantoderm KDMF as part of the drug registration process and uses the information provided in the Pantoderm KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pantoderm 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 Pantoderm API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pantoderm suppliers with KDMF on PharmaCompass.
