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.
01 1Cabergoline
01 1Israel
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
A Cabergoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cabergoline, including repackagers and relabelers. The FDA regulates Cabergoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cabergoline 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 Cabergoline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cabergoline supplier is an individual or a company that provides Cabergoline active pharmaceutical ingredient (API) or Cabergoline finished formulations upon request. The Cabergoline suppliers may include Cabergoline API manufacturers, exporters, distributors and traders.
click here to find a list of Cabergoline 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 Cabergoline Drug Master File in Japan (Cabergoline JDMF) empowers Cabergoline 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 Cabergoline JDMF during the approval evaluation for pharmaceutical products. At the time of Cabergoline 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 Cabergoline suppliers with JDMF on PharmaCompass.
We have 1 companies offering Cabergoline
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