DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Amgen Singapore Manufacturing Pte. Ltd
03 1HAS Healthcare Advanced Synthesis SA
04 1MSN Laboratories Private Limited
05 1Sionc Pharmaceuticals Pvt. Ltd
06 1Sterling Wisconsin, LLC
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registrant Name : Pamire Co., Ltd.
Registration Date : 2026-04-30
Registration Number : Su574-35-ND
Manufacturer Name : Dr. Reddy's Laboratories Lim...
Manufacturer Address : Unit I, Plot No. 137, 138, 145 & 146, Sri Venkateswara Co-operative industrial estate...
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PharmaCompass offers a list of Carfilzomib API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Carfilzomib manufacturer or Carfilzomib supplier for your needs.
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A PX-171-007 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PX-171-007, including repackagers and relabelers. The FDA regulates PX-171-007 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PX-171-007 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 PX-171-007 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A PX-171-007 supplier is an individual or a company that provides PX-171-007 active pharmaceutical ingredient (API) or PX-171-007 finished formulations upon request. The PX-171-007 suppliers may include PX-171-007 API manufacturers, exporters, distributors and traders.
click here to find a list of PX-171-007 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a PX-171-007 Drug Master File in Korea (PX-171-007 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of PX-171-007. The MFDS reviews the PX-171-007 KDMF as part of the drug registration process and uses the information provided in the PX-171-007 KDMF to evaluate the safety and efficacy of the drug.
After submitting a PX-171-007 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their PX-171-007 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of PX-171-007 suppliers with KDMF on PharmaCompass.
We have 6 companies offering PX-171-007
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