Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1M/s. Cohance Lifesciences Limited
01 1Oxolamine Citrate IH
01 1WC-0150N
01 1India
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Date of Issue : 2025-07-24
Valid Till : 2028-07-21
Written Confirmation Number : WC-0150N
Address of the Firm : API Unit-l, R.S. No. 50/1, Mukteswarapuram Village,\r\nJaggaiahpet Mandal, NTR D...
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PharmaCompass also assists you with knowing the Oxolamine Citrate API Price utilized in the formulation of products. Oxolamine Citrate API Price is not always fixed or binding as the Oxolamine Citrate Price is obtained through a variety of data sources. The Oxolamine Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bredon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bredon, including repackagers and relabelers. The FDA regulates Bredon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bredon 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 Bredon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bredon supplier is an individual or a company that provides Bredon active pharmaceutical ingredient (API) or Bredon finished formulations upon request. The Bredon suppliers may include Bredon API manufacturers, exporters, distributors and traders.
click here to find a list of Bredon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bredon written confirmation (Bredon WC) is an official document issued by a regulatory agency to a Bredon manufacturer, verifying that the manufacturing facility of a Bredon active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bredon APIs or Bredon finished pharmaceutical products to another nation, regulatory agencies frequently require a Bredon WC (written confirmation) as part of the regulatory process.
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