01 1Divi’s Laboratories
02 1M/s. Glochem Industries Ltd
01 1Levodopa (IP/BP/USP/Ph. Eur)
02 1Levodopa (IP/USP/BP/Ph. Eur.)
01 1WC-0029
02 1WC-0030
01 2India
Date of Issue : 2019-06-17
Valid Till : 2022-06-16
Written Confirmation Number : WC-0030
Address of the Firm : Unit-II, Annavaram(Post), Chippada Village, Beemunipatnam Mandal, Visakhapatan...
Date of Issue : 2013-06-11
Valid Till : 2016-06-05
Written Confirmation Number : WC-0029
Address of the Firm : Unit-II, Sy. No. 36, 37 and 46, Plot No. 77, J. N. Pharmacity, Thanam (V), Paraw...
A CAS-59-92-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-59-92-7, including repackagers and relabelers. The FDA regulates CAS-59-92-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-59-92-7 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 CAS-59-92-7 supplier is an individual or a company that provides CAS-59-92-7 active pharmaceutical ingredient (API) or CAS-59-92-7 finished formulations upon request. The CAS-59-92-7 suppliers may include CAS-59-92-7 API manufacturers, exporters, distributors and traders.
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A CAS-59-92-7 written confirmation (CAS-59-92-7 WC) is an official document issued by a regulatory agency to a CAS-59-92-7 manufacturer, verifying that the manufacturing facility of a CAS-59-92-7 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CAS-59-92-7 APIs or CAS-59-92-7 finished pharmaceutical products to another nation, regulatory agencies frequently require a CAS-59-92-7 WC (written confirmation) as part of the regulatory process.
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