01 1SM Biomed SDN.BHD.
01 1Sale Pharmaceutical Co., Ltd.
01 1Erythromycin
01 1Malaysia
Registrant Name : Sale Pharmaceutical 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, Price,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.
PharmaCompass also assists you with knowing the Erythromycin API Price utilized in the formulation of products. Erythromycin API Price is not always fixed or binding as the Erythromycin Price is obtained through a variety of data sources. The Erythromycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Propiocine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propiocine, including repackagers and relabelers. The FDA regulates Propiocine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propiocine 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 Propiocine supplier is an individual or a company that provides Propiocine active pharmaceutical ingredient (API) or Propiocine finished formulations upon request. The Propiocine suppliers may include Propiocine API manufacturers, exporters, distributors and traders.
click here to find a list of Propiocine 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 Propiocine Drug Master File in Korea (Propiocine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Propiocine. The MFDS reviews the Propiocine KDMF as part of the drug registration process and uses the information provided in the Propiocine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Propiocine 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 Propiocine API can apply through the Korea Drug Master File (KDMF).
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