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