01 1PolyPeptide Laboratories (Sweden) AB
01 1Felypressin
01 1Switzerland
Registration Number : 220MF10039
Registrant's Address : Ho(¨)gerudsgatan 21, Limhamn
Initial Date of Registration : 2008-02-05
Latest Date of Registration : 2008-02-05
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PharmaCompass offers a list of Felypressin 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 Felypressin manufacturer or Felypressin supplier for your needs.
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A Felypressine [INN-French] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Felypressine [INN-French], including repackagers and relabelers. The FDA regulates Felypressine [INN-French] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Felypressine [INN-French] 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 Felypressine [INN-French] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Felypressine [INN-French] supplier is an individual or a company that provides Felypressine [INN-French] active pharmaceutical ingredient (API) or Felypressine [INN-French] finished formulations upon request. The Felypressine [INN-French] suppliers may include Felypressine [INN-French] API manufacturers, exporters, distributors and traders.
click here to find a list of Felypressine [INN-French] 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 Felypressine [INN-French] Drug Master File in Japan (Felypressine [INN-French] JDMF) empowers Felypressine [INN-French] 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 Felypressine [INN-French] JDMF during the approval evaluation for pharmaceutical products. At the time of Felypressine [INN-French] 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 Felypressine [INN-French] suppliers with JDMF on PharmaCompass.
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