01 1M/s Melody Healthcare Pvt Ltd
01 1Levosimedan IH
01 1WC-0227n
01 1India
Date of Issue : 2022-07-28
Valid Till : 2025-07-02
Written Confirmation Number : WC-0227n
Address of the Firm : Plot No. J-73, MIDC, Tarapur, Boisar, Dist- Palghar 401506, Maharashtra, India
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PharmaCompass offers a list of Levosimendan 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 Levosimendan manufacturer or Levosimendan supplier for your needs.
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PharmaCompass also assists you with knowing the Levosimendan API Price utilized in the formulation of products. Levosimendan API Price is not always fixed or binding as the Levosimendan Price is obtained through a variety of data sources. The Levosimendan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Simdax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Simdax, including repackagers and relabelers. The FDA regulates Simdax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Simdax 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 Simdax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Simdax supplier is an individual or a company that provides Simdax active pharmaceutical ingredient (API) or Simdax finished formulations upon request. The Simdax suppliers may include Simdax API manufacturers, exporters, distributors and traders.
click here to find a list of Simdax suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Simdax written confirmation (Simdax WC) is an official document issued by a regulatory agency to a Simdax manufacturer, verifying that the manufacturing facility of a Simdax active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Simdax APIs or Simdax finished pharmaceutical products to another nation, regulatory agencies frequently require a Simdax WC (written confirmation) as part of the regulatory process.
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