01 1M/s. Hemmo Pharmaceuticals Pvt. Ltd
01 1Buserelin (Ph.Eur.)
01 1WC-0237
01 1India
Date of Issue : 2019-09-03
Valid Till : 2022-09-02
Written Confirmation Number : WC-0237
Address of the Firm : C-43, MIDC, TTC Industrial Area, Turbhe, Off Thane Belapur Road, Dist: Thane Mah...
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PharmaCompass offers a list of Buserelin Acetate 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 Buserelin Acetate manufacturer or Buserelin Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Buserelin Acetate API Price utilized in the formulation of products. Buserelin Acetate API Price is not always fixed or binding as the Buserelin Acetate Price is obtained through a variety of data sources. The Buserelin Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Suprefact manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Suprefact, including repackagers and relabelers. The FDA regulates Suprefact manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Suprefact 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 Suprefact manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Suprefact supplier is an individual or a company that provides Suprefact active pharmaceutical ingredient (API) or Suprefact finished formulations upon request. The Suprefact suppliers may include Suprefact API manufacturers, exporters, distributors and traders.
click here to find a list of Suprefact suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Suprefact written confirmation (Suprefact WC) is an official document issued by a regulatory agency to a Suprefact manufacturer, verifying that the manufacturing facility of a Suprefact active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Suprefact APIs or Suprefact finished pharmaceutical products to another nation, regulatory agencies frequently require a Suprefact WC (written confirmation) as part of the regulatory process.
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