Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1M/s Cohance Lifesciences Limited
01 1Levomepromazine Maleate BP/EP
01 1WC-0195
01 1India
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Date of Issue : 2022-08-25
Valid Till : 2025-02-07
Written Confirmation Number : WC-0195
Address of the Firm : Plot No. 3102/B, GIDC Estate Ankleshwar, Bharuch-393002, Gujarat, India
69
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A Tisercin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tisercin, including repackagers and relabelers. The FDA regulates Tisercin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tisercin 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 Tisercin supplier is an individual or a company that provides Tisercin active pharmaceutical ingredient (API) or Tisercin finished formulations upon request. The Tisercin suppliers may include Tisercin API manufacturers, exporters, distributors and traders.
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A Tisercin written confirmation (Tisercin WC) is an official document issued by a regulatory agency to a Tisercin manufacturer, verifying that the manufacturing facility of a Tisercin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tisercin APIs or Tisercin finished pharmaceutical products to another nation, regulatory agencies frequently require a Tisercin WC (written confirmation) as part of the regulatory process.
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