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 : 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
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
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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 Cerazette manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cerazette, including repackagers and relabelers. The FDA regulates Cerazette manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cerazette 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 Cerazette manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cerazette supplier is an individual or a company that provides Cerazette active pharmaceutical ingredient (API) or Cerazette finished formulations upon request. The Cerazette suppliers may include Cerazette API manufacturers, exporters, distributors and traders.
click here to find a list of Cerazette 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 Cerazette Drug Master File in Japan (Cerazette JDMF) empowers Cerazette 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 Cerazette JDMF during the approval evaluation for pharmaceutical products. At the time of Cerazette 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 Cerazette suppliers with JDMF on PharmaCompass.
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