TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1TAPI Czech Industries s. r. o.
01 1Pergolide mesylate
01 1Israel
TAPI offers customized CDMO Solutions for API development and manufacturing services.
Registration Number : 218MF10839
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2006-10-20
A Pergolide Mesylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pergolide Mesylate, including repackagers and relabelers. The FDA regulates Pergolide Mesylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pergolide Mesylate 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 Pergolide Mesylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pergolide Mesylate supplier is an individual or a company that provides Pergolide Mesylate active pharmaceutical ingredient (API) or Pergolide Mesylate finished formulations upon request. The Pergolide Mesylate suppliers may include Pergolide Mesylate API manufacturers, exporters, distributors and traders.
click here to find a list of Pergolide Mesylate 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 Pergolide Mesylate Drug Master File in Japan (Pergolide Mesylate JDMF) empowers Pergolide Mesylate 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 Pergolide Mesylate JDMF during the approval evaluation for pharmaceutical products. At the time of Pergolide Mesylate 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 Pergolide Mesylate suppliers with JDMF on PharmaCompass.
We have 1 companies offering Pergolide Mesylate
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