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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Everolimus manufacturer or Everolimus supplier.
PharmaCompass also assists you with knowing the Everolimus API Price utilized in the formulation of products. Everolimus API Price is not always fixed or binding as the Everolimus Price is obtained through a variety of data sources. The Everolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RAD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RAD, including repackagers and relabelers. The FDA regulates RAD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RAD 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 RAD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RAD supplier is an individual or a company that provides RAD active pharmaceutical ingredient (API) or RAD finished formulations upon request. The RAD suppliers may include RAD API manufacturers, exporters, distributors and traders.
click here to find a list of RAD 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 RAD Drug Master File in Korea (RAD KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of RAD. The MFDS reviews the RAD KDMF as part of the drug registration process and uses the information provided in the RAD KDMF to evaluate the safety and efficacy of the drug.
After submitting a RAD 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 RAD API can apply through the Korea Drug Master File (KDMF).
click here to find a list of RAD suppliers with KDMF on PharmaCompass.
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