Aspen API. More than just an API™
01 1Aspen Oss B. V.
01 1Asenapine maleate
01 1Netherlands
Aspen API. More than just an API™
Registration Number : 227MF10107
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2015-04-09
Latest Date of Registration : 2020-11-30
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PharmaCompass offers a list of Asenapine Maleate 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 Asenapine Maleate manufacturer or Asenapine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Asenapine Maleate API Price utilized in the formulation of products. Asenapine Maleate API Price is not always fixed or binding as the Asenapine Maleate Price is obtained through a variety of data sources. The Asenapine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A saphris manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of saphris, including repackagers and relabelers. The FDA regulates saphris manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. saphris 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 saphris manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A saphris supplier is an individual or a company that provides saphris active pharmaceutical ingredient (API) or saphris finished formulations upon request. The saphris suppliers may include saphris API manufacturers, exporters, distributors and traders.
click here to find a list of saphris 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 saphris Drug Master File in Japan (saphris JDMF) empowers saphris 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 saphris JDMF during the approval evaluation for pharmaceutical products. At the time of saphris 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 saphris suppliers with JDMF on PharmaCompass.
