DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddys Laboratories Limited
01 1Lomustine EP
01 1WC-0039n
01 1India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-05-26
Valid Till : 2025-07-07
Written Confirmation Number : WC-0039n
Address of the Firm : Unit-l, Plot Nos., 137,138,145 & 146, Sri Venkateswara Cooperative Industrial Es...
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A ICIG 1109 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ICIG 1109, including repackagers and relabelers. The FDA regulates ICIG 1109 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ICIG 1109 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 ICIG 1109 supplier is an individual or a company that provides ICIG 1109 active pharmaceutical ingredient (API) or ICIG 1109 finished formulations upon request. The ICIG 1109 suppliers may include ICIG 1109 API manufacturers, exporters, distributors and traders.
click here to find a list of ICIG 1109 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ICIG 1109 written confirmation (ICIG 1109 WC) is an official document issued by a regulatory agency to a ICIG 1109 manufacturer, verifying that the manufacturing facility of a ICIG 1109 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting ICIG 1109 APIs or ICIG 1109 finished pharmaceutical products to another nation, regulatory agencies frequently require a ICIG 1109 WC (written confirmation) as part of the regulatory process.
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