TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API India Private Limited
01 1Caspofungin acetate “Teva”
01 1Israel
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 305MF10081
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2023-07-12
Latest Date of Registration : 2023-07-12
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PharmaCompass offers a list of Caspofungin 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 Caspofungin manufacturer or Caspofungin supplier for your needs.
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A MolPort-029-887-122 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-029-887-122, including repackagers and relabelers. The FDA regulates MolPort-029-887-122 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-029-887-122 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A MolPort-029-887-122 supplier is an individual or a company that provides MolPort-029-887-122 active pharmaceutical ingredient (API) or MolPort-029-887-122 finished formulations upon request. The MolPort-029-887-122 suppliers may include MolPort-029-887-122 API manufacturers, exporters, distributors and traders.
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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 MolPort-029-887-122 Drug Master File in Japan (MolPort-029-887-122 JDMF) empowers MolPort-029-887-122 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 MolPort-029-887-122 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-029-887-122 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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