DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr Reddy's Laboratories Limited
01 1Liraglutide IH
01 1WC-0067
01 1India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-07
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
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A Liraglutide Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liraglutide Acetate, including repackagers and relabelers. The FDA regulates Liraglutide Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liraglutide 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 Liraglutide Acetate supplier is an individual or a company that provides Liraglutide Acetate active pharmaceutical ingredient (API) or Liraglutide Acetate finished formulations upon request. The Liraglutide Acetate suppliers may include Liraglutide Acetate API manufacturers, exporters, distributors and traders.
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A Liraglutide Acetate written confirmation (Liraglutide Acetate WC) is an official document issued by a regulatory agency to a Liraglutide Acetate manufacturer, verifying that the manufacturing facility of a Liraglutide Acetate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Liraglutide Acetate APIs or Liraglutide Acetate finished pharmaceutical products to another nation, regulatory agencies frequently require a Liraglutide Acetate WC (written confirmation) as part of the regulatory process.
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