DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s. Dr. Reddy’s Laboratories Limited
02 1M/S BDR Lifesciences
03 1M/s BDR Lifesciences Pvt Ltd
04 1M/s GLAND CHEMICALS PRIVATE LIMITED
05 1M/s Natco Organics Limited
06 1M/s Parabolic Drugs Ltd
07 1M/s Sionc Phamaceuticals Pvt Ltd
08 1M/s. Fresenius Kabi Oncology Ltd.,
09 1M/s. Hetro Labs Limited
10 1M/s. Laurus Labs Pvt. Ltd.,
11 1M/s. Reliance Life Sciences Pvt. Ltd.
12 1M/s. Shilpa Medicare Ltd.,
13 1M/s. Sun Pharmaceuticals Industries Ltd.
14 1MSN Laboratories Pvt. Ltd.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-06
Valid Till : 2025-07-07
Written Confirmation Number : WC-0039
Address of the Firm : Unit-I, Plot Nos.137, 138, 145 & 146, Sri Venkateswara Co- Operative Industrial ...
A Bortezomib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bortezomib, including repackagers and relabelers. The FDA regulates Bortezomib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bortezomib 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 Bortezomib supplier is an individual or a company that provides Bortezomib active pharmaceutical ingredient (API) or Bortezomib finished formulations upon request. The Bortezomib suppliers may include Bortezomib API manufacturers, exporters, distributors and traders.
click here to find a list of Bortezomib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bortezomib written confirmation (Bortezomib WC) is an official document issued by a regulatory agency to a Bortezomib manufacturer, verifying that the manufacturing facility of a Bortezomib active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bortezomib APIs or Bortezomib finished pharmaceutical products to another nation, regulatory agencies frequently require a Bortezomib WC (written confirmation) as part of the regulatory process.
click here to find a list of Bortezomib suppliers with Written Confirmation (WC) on PharmaCompass.
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