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01 1PolyPeptide Laboratories (Sweden) AB
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01 1Felypressin
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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, Price,and more, enabling you to easily find the right Felypressin manufacturer or Felypressin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Felypressin manufacturer or Felypressin supplier.
PharmaCompass also assists you with knowing the Felypressin API Price utilized in the formulation of products. Felypressin API Price is not always fixed or binding as the Felypressin Price is obtained through a variety of data sources. The Felypressin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Felipresina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Felipresina, including repackagers and relabelers. The FDA regulates Felipresina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Felipresina 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 Felipresina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Felipresina supplier is an individual or a company that provides Felipresina active pharmaceutical ingredient (API) or Felipresina finished formulations upon request. The Felipresina suppliers may include Felipresina API manufacturers, exporters, distributors and traders.
click here to find a list of Felipresina 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 Felipresina Drug Master File in Japan (Felipresina JDMF) empowers Felipresina 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 Felipresina JDMF during the approval evaluation for pharmaceutical products. At the time of Felipresina 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 Felipresina suppliers with JDMF on PharmaCompass.
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