01 1M/s. Hetro Labs Limited
02 1M/s. Natco Pharma Ltd,
03 1MSN Laboratories Pvt. Ltd.
01 2Regorafenib IH
02 1Regorafenib IHS
01 1WC-0014
02 1WC-0041
03 1WC-0349
01 3India
Date of Issue : 2022-09-16
Valid Till : 2025-08-08
Written Confirmation Number : WC-0041
Address of the Firm : Unit-I, Survey No.10, I.D.A, Gaddapotharam Village, Jinnaram Mandal,Medak Dist, ...
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm : MIs. MSN Laboratories Private Limited, Unit-II, sv. No, 50, Kardanur (Village), ...
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0014
Address of the Firm : Mekaguda (V) kothur (M) Mahabood nagar Dist, Telangana State India
A Regorafenib Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Regorafenib Monohydrate, including repackagers and relabelers. The FDA regulates Regorafenib Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Regorafenib Monohydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Regorafenib Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Regorafenib Monohydrate supplier is an individual or a company that provides Regorafenib Monohydrate active pharmaceutical ingredient (API) or Regorafenib Monohydrate finished formulations upon request. The Regorafenib Monohydrate suppliers may include Regorafenib Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Regorafenib Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Regorafenib Monohydrate written confirmation (Regorafenib Monohydrate WC) is an official document issued by a regulatory agency to a Regorafenib Monohydrate manufacturer, verifying that the manufacturing facility of a Regorafenib Monohydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Regorafenib Monohydrate APIs or Regorafenib Monohydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Regorafenib Monohydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Regorafenib Monohydrate suppliers with Written Confirmation (WC) on PharmaCompass.
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