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