01 2PolyPeptide Laboratories (Sweden) AB
01 2Desmopressin
01 2Switzerland
Registration Number : 224MF10122
Registrant's Address : Ho(¨)gerudsgatan 21, Limhamn
Initial Date of Registration : 2012-07-09
Latest Date of Registration : 2023-06-28
Registration Number : 306MF10047
Registrant's Address : Ho(¨)gerudsgatan 21, Limhamn
Initial Date of Registration : 2024-03-27
Latest Date of Registration : 2024-03-27
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PharmaCompass offers a list of Desmopressin Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Desmopressin Acetate manufacturer or Desmopressin Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desmopressin Acetate manufacturer or Desmopressin Acetate supplier.
A Stimate Nasal Spray manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stimate Nasal Spray, including repackagers and relabelers. The FDA regulates Stimate Nasal Spray manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stimate Nasal Spray 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 Stimate Nasal Spray manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Stimate Nasal Spray supplier is an individual or a company that provides Stimate Nasal Spray active pharmaceutical ingredient (API) or Stimate Nasal Spray finished formulations upon request. The Stimate Nasal Spray suppliers may include Stimate Nasal Spray API manufacturers, exporters, distributors and traders.
click here to find a list of Stimate Nasal Spray suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Stimate Nasal Spray Drug Master File in Japan (Stimate Nasal Spray JDMF) empowers Stimate Nasal Spray 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 Stimate Nasal Spray JDMF during the approval evaluation for pharmaceutical products. At the time of Stimate Nasal Spray 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 Stimate Nasal Spray suppliers with JDMF on PharmaCompass.
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