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...
A Buserelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buserelin, including repackagers and relabelers. The FDA regulates Buserelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buserelin 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 Buserelin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Buserelin supplier is an individual or a company that provides Buserelin active pharmaceutical ingredient (API) or Buserelin finished formulations upon request. The Buserelin suppliers may include Buserelin API manufacturers, exporters, distributors and traders.
click here to find a list of Buserelin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Buserelin written confirmation (Buserelin WC) is an official document issued by a regulatory agency to a Buserelin manufacturer, verifying that the manufacturing facility of a Buserelin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Buserelin APIs or Buserelin finished pharmaceutical products to another nation, regulatory agencies frequently require a Buserelin WC (written confirmation) as part of the regulatory process.
click here to find a list of Buserelin suppliers with Written Confirmation (WC) on PharmaCompass.
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