EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI ITALY S. r. l.
02 2CKD Bio Corporation
03 1Dong Kook Pharmaceutical Co. , Ltd.
01 4Teicoplanin
01 1France
02 3South Korea
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 226MF10148
Registrant's Address : Via Angelo Titi, 22/26, Zona ex punto franco, 72100 Brindisi, Italy
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2020-03-02
Registration Number : 223MF10162
Registrant's Address : 8, Chungjeong-ro, Seodaemun-gu, Seoul 120-756, Republic of Korea
Initial Date of Registration : 2011-11-14
Latest Date of Registration : 2011-11-14
Registration Number : 304MF10085
Registrant's Address : 8, Chungjeong-ro, Seodaemun-gu, Seoul, Republic of Korea
Initial Date of Registration : 2022-06-08
Latest Date of Registration : 2022-06-08
Registration Number : 219MF10354
Registrant's Address : 7, Teheran-ro 108-gil, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2020-12-07
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PharmaCompass offers a list of Teicoplanin 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 Teicoplanin manufacturer or Teicoplanin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Teicoplanin manufacturer or Teicoplanin supplier.
PharmaCompass also assists you with knowing the Teicoplanin API Price utilized in the formulation of products. Teicoplanin API Price is not always fixed or binding as the Teicoplanin Price is obtained through a variety of data sources. The Teicoplanin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Teicoplanin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teicoplanin, including repackagers and relabelers. The FDA regulates Teicoplanin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teicoplanin 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 Teicoplanin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Teicoplanin supplier is an individual or a company that provides Teicoplanin active pharmaceutical ingredient (API) or Teicoplanin finished formulations upon request. The Teicoplanin suppliers may include Teicoplanin API manufacturers, exporters, distributors and traders.
click here to find a list of Teicoplanin 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 Teicoplanin Drug Master File in Japan (Teicoplanin JDMF) empowers Teicoplanin 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 Teicoplanin JDMF during the approval evaluation for pharmaceutical products. At the time of Teicoplanin 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 Teicoplanin suppliers with JDMF on PharmaCompass.
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