01 1HETERO DRUGS LIMITED.
02 1JEIL PHARMACEUTICAL CO. , LTD.
03 1KUKJEON PHARMACEUTICAL Co. , Ltd.
01 2Cinacalcet Hydrochloride
02 1Cinacalcet hydrochloride
01 1India
02 2South Korea
Registration Number : 230MF10003
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2018-01-10
Latest Date of Registration : 2018-01-10
Registration Number : 301MF10033
Registrant's Address : 343, Sapyeong-daero, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2019-07-19
Latest Date of Registration : 2019-07-19
Registration Number : 230MF10125
Registrant's Address : #1516, Geumgang Penterium IT Tower, 282, Hagui-ro, Dongan-gu, Anyang-si, Gyeonggi-do,...
Initial Date of Registration : 2018-09-03
Latest Date of Registration : 2020-03-02
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PharmaCompass offers a list of Cinacalcet Hydrochloride 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 Cinacalcet Hydrochloride manufacturer or Cinacalcet Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cinacalcet Hydrochloride manufacturer or Cinacalcet Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cinacalcet Hydrochloride API Price utilized in the formulation of products. Cinacalcet Hydrochloride API Price is not always fixed or binding as the Cinacalcet Hydrochloride Price is obtained through a variety of data sources. The Cinacalcet Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Regpara manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Regpara, including repackagers and relabelers. The FDA regulates Regpara manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Regpara 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 Regpara manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Regpara supplier is an individual or a company that provides Regpara active pharmaceutical ingredient (API) or Regpara finished formulations upon request. The Regpara suppliers may include Regpara API manufacturers, exporters, distributors and traders.
click here to find a list of Regpara suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Regpara Drug Master File in Japan (Regpara JDMF) empowers Regpara API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Regpara JDMF during the approval evaluation for pharmaceutical products. At the time of Regpara JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Regpara suppliers with JDMF on PharmaCompass.
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