TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI Czech Industries s. r. o.
02 1YS Life Science Co. , Ltd.
01 2Cabergoline
01 1Israel
02 1South Korea
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 217MF11279
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2010-07-09
Registration Number : 307MF10053
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2025-04-08
Latest Date of Registration : 2025-04-08
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PharmaCompass offers a list of Cabergoline API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Cabergoline manufacturer or Cabergoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cabergoline manufacturer or Cabergoline supplier.
A D00987 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D00987, including repackagers and relabelers. The FDA regulates D00987 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D00987 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 D00987 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A D00987 supplier is an individual or a company that provides D00987 active pharmaceutical ingredient (API) or D00987 finished formulations upon request. The D00987 suppliers may include D00987 API manufacturers, exporters, distributors and traders.
click here to find a list of D00987 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 D00987 Drug Master File in Japan (D00987 JDMF) empowers D00987 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 D00987 JDMF during the approval evaluation for pharmaceutical products. At the time of D00987 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 D00987 suppliers with JDMF on PharmaCompass.
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