01 1ERREGIERRE S. p. A.
01 1URAAPIDIL
01 1Italy
Registration Number : 304MF10127
Registrant's Address : VIA F. BARACCA 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2022-08-31
Latest Date of Registration : 2022-08-31
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PharmaCompass offers a list of Urapidil Hydrochloride 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 Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier.
PharmaCompass also assists you with knowing the Urapidil Hydrochloride API Price utilized in the formulation of products. Urapidil Hydrochloride API Price is not always fixed or binding as the Urapidil Hydrochloride Price is obtained through a variety of data sources. The Urapidil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Uraprene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uraprene, including repackagers and relabelers. The FDA regulates Uraprene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uraprene 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 Uraprene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Uraprene supplier is an individual or a company that provides Uraprene active pharmaceutical ingredient (API) or Uraprene finished formulations upon request. The Uraprene suppliers may include Uraprene API manufacturers, exporters, distributors and traders.
click here to find a list of Uraprene 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 Uraprene Drug Master File in Japan (Uraprene JDMF) empowers Uraprene 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 Uraprene JDMF during the approval evaluation for pharmaceutical products. At the time of Uraprene 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 Uraprene suppliers with JDMF on PharmaCompass.
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