01 3Biocon Limited
02 1BrightGene Pharmaceutical Co. Ltd@[Sirolimus Manufacturer]BrightGene Fine Chemical Co., Ltd
03 1Chong Kun Dang Bio Co., Ltd @ ['Sirolimus' manufacturing plant] Zhejiang Wild Wind Pharmaceutical Co., Ltd
04 1Chong Kun Dang Bio Co., Ltd. @ [Starting material 'sirolimus' manufacturing plant] Zhejiang Wild Wind Pharmaceutical Co., Ltd. @ Chong Kun Dang Bio Co., Ltd.
05 1Concord Biotech Limited
06 1Novartis Pharma Schweizerhalle AG.@[Partial process contract manufacturing (manufacturer)](Blending process) Novartis Pharma AG@[Partial process contract manufacturing (manufacturer)](Blending process) Novartis Pharmaceutical Manufacturing LLC@[Partial pr
07 1Novartis Pharmaceutical Manufacturing LLC. (Full Process) @ [Mixed Process Manufacturing Plant 1] Novartis Pharma AG @ [Mixed Process Manufacturing Plant 2] Novartis Pharma Stein AG
08 1[Partial process contract manufacturing (manufacturing requester)] (synthesis and blending process) Novartis Pharma AG@[Partial process contract manufacturing (manufacturer)] (blending process) Novartis Pharmaceutical Manufacturing LLC@[Partial process co
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PharmaCompass offers a list of Everolimus API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Everolimus manufacturer or Everolimus supplier for your needs.
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A CAS-159351-69-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-159351-69-6, including repackagers and relabelers. The FDA regulates CAS-159351-69-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-159351-69-6 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 CAS-159351-69-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CAS-159351-69-6 supplier is an individual or a company that provides CAS-159351-69-6 active pharmaceutical ingredient (API) or CAS-159351-69-6 finished formulations upon request. The CAS-159351-69-6 suppliers may include CAS-159351-69-6 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-159351-69-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 CAS-159351-69-6 Drug Master File in Korea (CAS-159351-69-6 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CAS-159351-69-6. The MFDS reviews the CAS-159351-69-6 KDMF as part of the drug registration process and uses the information provided in the CAS-159351-69-6 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CAS-159351-69-6 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 CAS-159351-69-6 API can apply through the Korea Drug Master File (KDMF).
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