01 1M/s. Hemmo Pharmaceuticals Pvt. Ltd
01 1Cetrorelix (IH)
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 Cetrorelix manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetrorelix, including repackagers and relabelers. The FDA regulates Cetrorelix manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetrorelix 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 Cetrorelix manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cetrorelix supplier is an individual or a company that provides Cetrorelix active pharmaceutical ingredient (API) or Cetrorelix finished formulations upon request. The Cetrorelix suppliers may include Cetrorelix API manufacturers, exporters, distributors and traders.
click here to find a list of Cetrorelix suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cetrorelix written confirmation (Cetrorelix WC) is an official document issued by a regulatory agency to a Cetrorelix manufacturer, verifying that the manufacturing facility of a Cetrorelix active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cetrorelix APIs or Cetrorelix finished pharmaceutical products to another nation, regulatory agencies frequently require a Cetrorelix WC (written confirmation) as part of the regulatory process.
click here to find a list of Cetrorelix suppliers with Written Confirmation (WC) on PharmaCompass.
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