Aspen API. More than just an API™
01 1Aspen Oss B. V.
02 3INDUSTRIALE CHIMICA s. r. l.
01 4Desogestrel
01 3Italy
02 1Netherlands
Aspen API. More than just an API™
Registration Number : 303MF10070
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2021-04-22
Latest Date of Registration : 2021-04-22
Registration Number : 230MF10041
Registrant's Address : Via E. H. Grieg, 13, 21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2018-02-28
Latest Date of Registration : 2018-02-28
Registration Number : 221MF10126
Registrant's Address : Via E. H. Greig, 13, 21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2009-06-23
Latest Date of Registration : 2009-06-23
Registration Number : 221MF10125
Registrant's Address : Via E. H. Greig, 13, 21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2009-06-23
Latest Date of Registration : 2009-06-23
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PharmaCompass offers a list of Desogestrel 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 Desogestrel manufacturer or Desogestrel supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desogestrel manufacturer or Desogestrel supplier.
PharmaCompass also assists you with knowing the Desogestrel API Price utilized in the formulation of products. Desogestrel API Price is not always fixed or binding as the Desogestrel Price is obtained through a variety of data sources. The Desogestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DB00304 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DB00304, including repackagers and relabelers. The FDA regulates DB00304 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DB00304 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 DB00304 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DB00304 supplier is an individual or a company that provides DB00304 active pharmaceutical ingredient (API) or DB00304 finished formulations upon request. The DB00304 suppliers may include DB00304 API manufacturers, exporters, distributors and traders.
click here to find a list of DB00304 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 DB00304 Drug Master File in Japan (DB00304 JDMF) empowers DB00304 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 DB00304 JDMF during the approval evaluation for pharmaceutical products. At the time of DB00304 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 DB00304 suppliers with JDMF on PharmaCompass.
We have 2 companies offering DB00304
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