EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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01 1EUROAPI ITALY S. r. l.
02 2CKD Bio Corporation
03 1Dong Kook Pharmaceutical Co. , Ltd.
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01 4Teicoplanin
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01 1France
02 3South Korea
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 : 715, Yeongdong-daero, 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 A2-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teicoplanin A2-5, including repackagers and relabelers. The FDA regulates Teicoplanin A2-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teicoplanin A2-5 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 A2-5 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Teicoplanin A2-5 supplier is an individual or a company that provides Teicoplanin A2-5 active pharmaceutical ingredient (API) or Teicoplanin A2-5 finished formulations upon request. The Teicoplanin A2-5 suppliers may include Teicoplanin A2-5 API manufacturers, exporters, distributors and traders.
click here to find a list of Teicoplanin A2-5 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 A2-5 Drug Master File in Japan (Teicoplanin A2-5 JDMF) empowers Teicoplanin A2-5 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 A2-5 JDMF during the approval evaluation for pharmaceutical products. At the time of Teicoplanin A2-5 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 A2-5 suppliers with JDMF on PharmaCompass.
We have 3 companies offering Teicoplanin A2-5
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