01 1Olon S. p. A.
01 1Pipamperon hydrochloride
01 1Italy
Registration Number : 227MF10280
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2015-12-11
Latest Date of Registration : 2022-07-06
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PharmaCompass offers a list of Pipamperone 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 Pipamperone manufacturer or Pipamperone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pipamperone manufacturer or Pipamperone supplier.
PharmaCompass also assists you with knowing the Pipamperone API Price utilized in the formulation of products. Pipamperone API Price is not always fixed or binding as the Pipamperone Price is obtained through a variety of data sources. The Pipamperone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dipiperon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dipiperon, including repackagers and relabelers. The FDA regulates Dipiperon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dipiperon 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 Dipiperon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dipiperon supplier is an individual or a company that provides Dipiperon active pharmaceutical ingredient (API) or Dipiperon finished formulations upon request. The Dipiperon suppliers may include Dipiperon API manufacturers, exporters, distributors and traders.
click here to find a list of Dipiperon 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 Dipiperon Drug Master File in Japan (Dipiperon JDMF) empowers Dipiperon 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 Dipiperon JDMF during the approval evaluation for pharmaceutical products. At the time of Dipiperon 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 Dipiperon suppliers with JDMF on PharmaCompass.
