Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1M/s. Cohance Lifesciences Limited
01 1Trimebutine Maleate Ph. Eur
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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A Debridat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Debridat, including repackagers and relabelers. The FDA regulates Debridat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Debridat 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 Debridat supplier is an individual or a company that provides Debridat active pharmaceutical ingredient (API) or Debridat finished formulations upon request. The Debridat suppliers may include Debridat API manufacturers, exporters, distributors and traders.
click here to find a list of Debridat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Debridat written confirmation (Debridat WC) is an official document issued by a regulatory agency to a Debridat manufacturer, verifying that the manufacturing facility of a Debridat active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Debridat APIs or Debridat finished pharmaceutical products to another nation, regulatory agencies frequently require a Debridat WC (written confirmation) as part of the regulatory process.
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